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| Vol 65, No 5 (2019) |
IgG4-associated disease in differential diagnosis of inflammatory orbitopathy |
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Yaroslav O. Grusha, Dilyara S. Ismailova, Natalya Yu. Sviridenko, Pavel I. Novikov, Alla M. Kovrigina |
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| Vol 65, No 5 (2019) |
Clinical case report: history of diagnosis and clinical features of type autoimmune polyglandular syndrome 1 |
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Viktoriya V. Troshina, Natalia Yu. Romanova, Leila S. Sozaeva, Ekaterina A. Troshina |
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| Vol 65, No 4 (2019) |
Virilizing ovarian tumor: the challenges of differential diagnosis |
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Marina F. Kalashnikova, Natalia V. Likhodey, Anatoly N. Tiulpakov, Evgeniya V. Fedorova, Dmitry V. Bryunin, Alla A. Bakhvalova, Maria A. Glushakova, Svetlana A. Smirnova, Valentin V. Fadeyev |
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| Vol 65, No 4 (2019) |
Secondary hyperaldosteronism and medullary nephrocalcinosis caused by self-administered and uncontrolled laxative use in an adolescent patient |
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Elena N. Sibileva, Nadezhda Yu. Mironova, Galina V. Korobitcina, Olga T. Koshlakova, Olga E. Ipatova |
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| Vol 65, No 4 (2019) |
Hypoglycemia in neonates: a review of the literature and a case report |
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Tatiana E. Taranushenko, Natalia G. Kiseleva, Olga V. Lazareva, Irina I. Kalygnaja |
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| Vol 65, No 4 (2019) |
A clinical case of combined differentiated thyroid cancer and primary hyperparathyroidism: the complexity of topical differential diagnosis |
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Konstantin Yu. Slashchuk, Mikhail V. Degtyarev, Sergey S. Serzhenko, Pavel O. Rumyantsev, Marina S. Sheremeta, Valentina S. Yasuchenia, Alexey A. Trukhin, Yaroslav I. Sirota, Olga D. Baranova, Petr A. Nikiforovich |
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| Vol 65, No 4 (2019) |
Somatic mutations in the androgen receptor gene as the cause of androgen insensitivity syndrome |
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Natalia Yu. Kalinchenko, Anna A. Kolodkina, Vasiliy M. Petrov, Evgeniy V. Vasiliev, Anatoly N. Tiulpakov |
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| Vol 65, No 4 (2019) |
An ovarian hyperstimulation syndrome caused by gonadotropinoma in a young woman |
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Anna M. Gorbacheva, Elena G. Przhiyalkovskaya, Vilen N. Azizyan, Irina V. Stanoevich, Andrey Yu. Grigoriev, Anna I. Sazonova, Anastasiya M. Lapshina, Zhanna E. Belaya |
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| Vol 65, No 3 (2019) |
Autoimmune polyglandular disorders in myotonic dystrophy |
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Ekaterina A. Troshina, Elena A. Panfilova, Taras S. Panevin |
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| Vol 65, No 2 (2019) |
Sustained ventricular tachycardia in a patient with a single ventricle of the heart and a pheochromocytoma |
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Konstantin V. Melkozerov, Alexander B. Kuznetsov, Victor Yu. Kalashnikov, Fatima М. Abdulkhabirova, Sergey N. Kuznetsov, Anna M. Gorbacheva, Ivan I. Dedov |
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| Vol 65, No 2 (2019) |
Manifestation of Graves’ disease, resulting from radiosurgical treatment of acromegaly, in a patient with panhypopituitarism |
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Ludmila I. Astafyeva, Pavel L. Kalinin, Tatyana A. Kienia, Valentin V. Fadeyev |
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| Vol 65, No 2 (2019) |
Hereditary Cushing’s syndrome caused by primary bilateral macronodular adrenal hyperplasia due to ARMC5 mutation with concomitant primary hyperparathyroidism: the first known case in Russia |
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Elizaveta O. Mamedova, Evgeny V. Vasilyev, Vasily M. Petrov, Natalya S. Izmailova, Svetlana A. Buryakina, Liudmila Ya. Rozhinskaya, Anatoly N. Tiulpakov, Zhanna E. Belaya |
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| Vol 65, No 2 (2019) |
Differential diagnosis between autoimmune thyrotoxicosis and thyroid hormone resistance syndrome: clinical case report |
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Natalya V. Mazurina, Ekaterina A. Troshina, Olga S. Chukhacheva |
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| Vol 65, No 1 (2019) |
Hypoglycemic syndrome in hepatic epithelioid hemangioendothelioma, successful treatment — liver transplantation from a living related donor |
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Irina A. Bondar, Ludmila I. Chesnochenko, Olesia Yu. Shabelnikova, Ivan A. Porshennikov |
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| Vol 65, No 1 (2019) |
Sodium balance impairment in a child with severe traumatic brain injury |
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Yuriy S. Aleksandrovich, Konstantin V. Pshenisnov, Anastasiya S. Ustinova, Vladimir V. Kopylov, Irina V. Aleksandrovich, Vladimir I. Gordeev |
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| Vol 65, No 1 (2019) |
Incomplete Wolfram syndrome. Clinical case report |
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Oleg A. Dianov, Ekaterina A. Lavrova, Vadim V. Maltcev, Darina A. Oleynik |
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| Vol 64, No 6 (2018) |
Chronic thyrotoxic myocarditis complicated by myocardial rupture in a patient with autoimmune thyroiditis |
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Natalya A. Cherkasova, Georgy O. Zairatyants, Natalya A. Ananitcheva, Svetlana E. Kolendo |
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| Vol 64, No 6 (2018) |
Phenotypes of endocrine ophthalmopathy: clinical manifestation and tomographic characteristics |
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Irina M. Belovalova, Natalya Yu. Sviridenko, Elena G. Bessmertnaya, Anna A. Chepurina, Marina S. Sheremeta, Alexander A. Mikheenkov |
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| Vol 64, No 5 (2018) |
Differential diagnosis of morphological forms of congenital hyperinsulinism using [18F]-DOPA PET/CT |
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Diliara N. Gubaeva, Maria A. Melikyan, Daria V. Ryzhkova, Lubov B. Mitrofanova, Irina L. Nikitina |
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| Vol 64, No 5 (2018) |
The first case of a rare form of isolated glucocorticoid insufficiency associated with to NNT gene mutation reported in the Russian Federation |
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Irina Y. Chernyak, Nataliya Y. Kalinchenko, Asiet I. Tlif, Elena I. Kleshenko, Evgeny V. Vasiliev, Vasily M. Petrov, Anatoly N. Tiulpakov |
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| Vol 64, No 5 (2018) |
Positron emission tomography in combination with computed tomography with 18F-fluorocholine in the topical diagnosis of parathyroid tumors and secondary changes in bone tissue associated with hyperparathyroid osteodystrophy: two case studies |
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Natalia G. Mokrysheva, Julia A. Krupinova, Mikhail B. Dolgushin, Akgul A. Odzharova, Iya A. Voronkova, Valeriy V. Voskoboynikov, Nikolaj S. Kuznecov |
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| Vol 64, No 4 (2018) |
A case of combination of two autoimmune diseases: type 1 diabetes mellitus and systemic scleroderma in a 13-year-old girl |
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Elena V. Titovich, Ekaterina A. Andrianova |
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| Vol 64, No 4 (2018) |
The features of cataract surgery in a patient with Graves’ disease and endocrine ophthalmopathy |
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Dmitry V. Lipatov, Natalya Yu. Sviridenko, Elena G. Bessmertnaya, Anna A. Tolkacheva |
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| Vol 64, No 3 (2018) |
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a case report |
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Elena B. Khramova, Elena Yu. Khorosheva, Olga V. Perfilova |
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| Vol 64, No 3 (2018) |
The rare form of congenital adrenal hyperplasia caused by an autosomal dominant form of STAR deficiency |
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Natalia Y. Kalinchenko, Galina V. Chistousova, Vasily M. Petrov, Evgeny V. Vasiliev, Anatoly N. Tiulpakov |
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| Vol 64, No 2 (2018) |
A familial case of insulin-dependent diabetes mellitus with a mutation in the PTF1A gene |
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Galina N. Svetlova, Tamara L. Kuraeva, Elena A. Sechko, Valentina A. Peterkova |
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| Vol 64, No 2 (2018) |
Problems of the differential diagnosis of MODY3 in obesity |
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Elena A. Sechko, Ekaterina A. Andrianova, Olga N. Ivanova, Tamara L. Kuraeva |
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| Vol 64, No 2 (2018) |
Late-diagnosed salt-wasting congenital adrenal hyperplasia in adult patient |
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Liudmila Ya. Rozhinskaya, Natalia Yu. Kalinchenko, Zhanna E. Belaya, Tatiana S. Zenkova, Alexander S. Lutsenko, Asiyat A. Bittirova |
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| Vol 64, No 1 (2018) |
Neonatal hypoglycemia in the De Morsier syndrome |
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Tatiana V. Kovalenko, Irina N. Petrova, Tatiana Yu. Tarasova |
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| Vol 64, No 1 (2018) |
Familial case of late diagnosis of Persistence of Müllerian derivatives syndrome type 1 |
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Natalia Yu. Kalinchenko, Dmitry N. Brovin, Irina B. Kostrova, Vasily M. Petrov, Evgeny V. Vasiliev, Anatoly N. Tiulpakov |
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| Vol 64, No 1 (2018) |
Disorder of sex development 46,XY associated with mutations in the gene MAP3K1. The report of clinical cases |
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Irina V. Kopylova, Elena S. Kuznetsova, Igor S. Chugunov, Elizaveta M. Orlova, Oleg S. Danilenko, Dmitry N. Brovin, Maria A. Kareva, Valentina A. Peterkova |
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| Vol 64, No 1 (2018) |
Familial case of normosmic hypogonadotropic hypogonadism with polydactyly, associated with defect of FGFR1 gene |
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Maria V. Gerasimova, Natalya U. Kalinchenko, Evgeniy V. Vasiliev, Vasiliy M. Petrov, Anatoly N. Tiulpakov |
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| Vol 63, No 6 (2017) |
Treatment of hypoparathyroidism with the recombinant parathyroid hormone (1—34) in a female patient with type 1 autoimmune polyglandular syndrome: the first experience in the Russian Federation |
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Leila S. Sozaeva, Elizaveta M. Orlova, Maria A. Kareva, Natalya Yu. Sviridenko, Natalya V. Molashenko, Anatoly G. Kuzmin, Valentina A. Peterkova |
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| Vol 63, No 5 (2017) |
Carbohydrate metabolism disorders in salicylate poisoning: diagnostic problems and physician’s tactics |
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Elena E. Petryaykina, Olga F. Vykhristyuk, Igor E. Koltunov |
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| Vol 63, No 5 (2017) |
A clinical case of hereditary papillary thyroid carcinoma associated with a germline DICER1 gene mutation |
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Svetlana A. Babinskaya, Natalia Yu. Kalinchenko, Alexey A. Ilyin, Natalia V. Severskaya, Irina V. Chebotareva, Kseniya S. Nizhegorodova, Pavel O. Rumyantsev, Anatoly N. Tiulpakov |
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| Vol 63, No 5 (2017) |
A case report of concomitant myopathy, adrenal insufficiency, and mental retardation linked with deletion of Xp21 |
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Elizaveta M. Orlova, Marina V. Kurkina, Leila S. Sozaeva, Maria A. Kareva, Ilya V. Kanivets, Anna A. Antonets, Ekaterina Yu. Zakharova |
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| Vol 63, No 5 (2017) |
Mediastinal teratoma with mature fetal pancreatic tissue, nesidioblastosis and focal hyperplasia of neuroendocrine cells. A case report |
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Pavel O. Rumyantsev, Aleksandr Yu. Abrosimov, Aleksandr S. Tertychnyi, Liliya S. Selivanova, Konstantin Yu. Slashchuk |
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| Vol 63, No 4 (2017) |
Large goiter in a patient with congenital hypothyroidism |
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Anna V. Bolmasova, Maria A. Melikyan, Elena A. Filippova, Marina V. Narogan, Yulia L. Podurovskaya, Anna N. Kotova |
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| Vol 63, No 4 (2017) |
The efficacy of dopamine agonist therapy in a young man with a giant prolactinoma: case report |
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Alexandr I. Tsiberkin, Tatiana L. Karonova, Anna B. Dalmatova, Elena N. Grineva |
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| Vol 63, No 2 (2017) |
HCG-secreting hepatoblastoma |
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Darya N. Koroleva, Tatiana S. Olina, Tatiana V. Kovalenko |
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| Vol 63, No 2 (2017) |
Glycogenosis type IX in a 9-year-old child |
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Nina V. Bolotova, Andrey P. Averyanov, Natalia Yu. Filina, Ekaterina Yu. Zaharova, Maria A. Melikyan, Olesya A. Velikotskaya, Tatyana V. Strokova, Yulia V. Paltseva |
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| Vol 63, No 2 (2017) |
Combination of lipoatrophic diabetes mellitus with systemic scleroderma and phenylketonuria |
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Galina N. Svetlova, Tamara L. Kuraeva, Dmitriy L. Alekseev, Valentina A. Peterkova |
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| Vol 63, No 2 (2017) |
Long-term follow-up of a child with Rabson—Mendenhall syndrome |
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Roza A. Atanesyan, Leonid Yu. Klimov, Tatyana M. Vdovina, Tatyana A. Uglova, Marina V. Stoyan, Viktoria A. Kuryaninova, Lilit S. Alaverdyan, Elena E. Krasilnikova, Rafael I. Arakelyan |
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| Vol 63, No 2 (2017) |
De la Chapelle syndrome: clinical and laboratory characteristics of 4 patients |
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Ekaterina S. Sannikova, Oleg Yu. Latyshev, Lubov N. Samsonova, Elena V. Kiseleva, Goar F. Okminyan, Elvira P. Kasatkina |
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| Vol 63, No 2 (2017) |
Growth and sexual retardation in a boy with celiac disease |
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Lubov B. Brzhezinski, Oleg Yu. Latyshev, Lubov N. Samsonova, Goar F. Okminyan, Elena V. Kiseleva, Elvira P. Kasatkina, Mihail I. Pykov |
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| Vol 63, No 2 (2017) |
A case of congenital hypothyroidism combined with sensorineural hearing loss (Pendred syndrome) caused by a TPO gene defect |
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Nina A. Makretskaya, Olga B. Bezlepkina, Olga A. Chikulaeva, Evgeny V. Vasilyev, Vasiliy M. Petrov, Ivan I. Dedov, Anatoly N. Tiulpakov |
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| Vol 63, No 2 (2017) |
Papillary thyroid cancer in an adolescent with a toxic single nodular goiter |
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Olga S. Rogova, Goar F. Okminyan, Lubov N. Samsonova, Elena V. Kiseleva, Oleg Yu. Latyshev, Natalja N. Egarmina, Elvira P. Kasatkina |
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| Vol 63, No 2 (2017) |
A case of nephrogenic syndrome of inappropriate antidiuresis caused by a mutation of the vasopressin type 2 receptor |
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Nadezhda V. Makazan, Natalia A. Zubkova, Anatolyi N. Tiulpakov |
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| Vol 63, No 2 (2017) |
Pseudohypertrophic myopathy in a child with hypothyroidism (Kocher—Debre—Semelaigne syndrome) |
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Elena A. Bogova, Tatyana Yu. Shiryaeva |
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| Vol 63, No 2 (2017) |
Masks of severe acquired hypothyroidism in preschool children |
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Irina L. Alimova, Yulia V. Labyzova |
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| Vol 63, No 2 (2017) |
Mutations in the ghrelin receptor gene GHSR in congenital hypopituitarism |
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Elena B. Bashnina, Olga S. Berseneva, Andrey S. Glotov, Oleg S. Glotov, Mariia E. Turkunova, Elena A. Serebryakova, Vladislav S. Baranov |
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| Vol 63, No 2 (2017) |
Cushing’s syndrome in an infant |
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Maria A. Kareva, Nadezda V. Makazan, Elizaveta M. Orlova, Igor V. Poddubnyi, Valentina A. Peterkova |
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| Vol 63, No 3 (2017) |
A novel heterozygous mutation in POU1F1 is associated with combined pituitary hormone deficiency |
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Anna E. Gavrilova, Elena V. Nagaeva, Olga Y. Rebrova, Tatiana Y. Shiryaeva, Anatoly N. Tiulpakov, Valentina A. Peterkova |
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| Vol 63, No 3 (2017) |
Insulin autoimmune syndrome: a rare cause of hypoglycemia. The case report of the syndrome in pediatric practice |
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Elena S. Kuznetsova, Oxana V. Pilipenko, Maria А. Melikyan |
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| Vol 63, No 3 (2017) |
The case of Crohn's disease in a child with congenital growth hormone deficiency. |
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Elena B. Bashnina, Olga S. Berseneva, Tatyana E. Korytko, Mariia E. Turkunova |
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| Vol 63, No 3 (2017) |
Hypopituitarism due to mutation in the PROP1 gene in association with the 47,XYY karyotype and autosomal dominant atrioventricular septal defect: two case reports |
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Dilyara N. Gubaeva, Elizaveta M. Orlova, Maria S. Pankratova, Alexander V. Vorontsov, Maria А. Kareva |
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| Vol 63, No 3 (2017) |
Ovotesticular disorder of sexual development in a patient with 46,XY karyotype |
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Nadezda Y. Raygorodskaya, Nina V. Bolotova, Danil A. Jarkov, Tatyana V. Palatova, Natalya S. Dorovskaya |
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| Vol 63, No 3 (2017) |
Hypoglycemia as a manifestation of congenital multiple pituitary hormone deficiency in patients without growth retardation: a clinical series |
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Maria A. Kareva, Elizaveta M. Orlova, Maria A. Melikyan, Alexandr V. Vorontsov, Victoria P. Vladimirova, Valentina A. Peterkova |
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| Vol 63, No 3 (2017) |
Familial case of congenital hyperinsulinism associated with mutation in the GLUD1 gene |
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Maria A. Melikyan, Anatoly N. Tiulpakov, Maria A. Kareva |
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| Vol 63, No 1 (2017) |
Thyrotoxic hepatitis |
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Dmitrij V. Pikulev, Aleksej V. Klemenov |
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| Vol 63, No 1 (2017) |
TSH-secreting pituitary adenoma: late diagnosis and effectiveness of therapy |
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Galina G. Petrik, Elena D. Kosmacheva, Ulya I. Polyakova, Svetlana V. Butaeva, Ludmila Ya. Rozhinskaya, Zhanna E. Belaya |
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| Vol 63, No 1 (2017) |
IDIOPATHIC INFANTILE HYPERCALCEMIA . DESCRIPTION OF CLINICAL CASES AND REVIEW. |
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Yulia V. Tikhonovich, Anna A. Kolodkina, Kristina S. Kulikova, Yulia Yu. Golubkina, Natalia Yu. Kalinchenko, Larisa V. Savelieva, Mikhail M. Kostik, Ludmila Y. Rozhinskaya, Anatoly N. Tiulpakov |
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| Vol 62, No 6 (2016) |
Three RET germ-line mutations in a family with multiple endocrine neoplasia type 2A syndrome |
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Natalia V Severskaya, Vladimir G Polyakov, Ruslan V Shishkov, Alexey A Ilin, Natalia V Ivanova, Alevtina I. Pavlovskaya, Valentina M. Kozlova, Faina A. Amosenko, Liudmila N. Lyubchenko, Tatyana P. Kazubskaya, Natalia A. Koshechkina, Elena V. Mikhailova, Irina I. Matveeva, Irina N. Serebryakova, Svetlana N. Mikhailova, Natalia Y. Kalinchenko |
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| Vol 62, No 3 (2016) |
Case of congenital hypothyroidism related to NKX2-1 |
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Nina A. Makretskaya, Natalya Y. Kalinchenko, Evgeny V. Vasiliev, Vasiliy M. Petrov, Anatoly N. Tiulpakov |
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| Vol 62, No 4 (2016) |
ACTH-producing medullary thyroid cancer. Clinical case. |
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Evgenia I. Marova, Ludmila Ya. Rozhinskaya, Iya A. Voronkova, Oleg V. Remizov, Anna I. Zavalishina, Konstantin Yu. Slashchuk, Mihail I. Davydov, Vitaliy Zh. Brzhezovsky, Sergey A. Gerasimov, Antonio K. Chekini, Dmitry K. Stelmach, Maksim B. Pak |
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| Vol 62, No 2 (2016) |
Description of the first genetically confirming case with Donahue’s syndrome in Russia |
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Yulia V. Tikhonovich, Oleg A. Malievsky, Anatoly Tyul'pakov |
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| Vol 62, No 3 (2016) |
Hereditary variant of diabetes mellitus caused by a defect of the NEUROD1 gene (MODY6): the first description in Russia |
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Olesya A. Gioeva, Anna A. Kolodkina, Evgeny V. Vasilyev, Vasiliy M. Petrov, Anatoly N. Tiulpakov |
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| Vol 62, No 3 (2016) |
Сushing’s syndrome in early infancy due to МcCune—Albright syndrome |
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Nadezhda V. Makazan, Elizaveta M. Orlova, Maria A. Kareva, Igor V. Poddybnyi, Kirill N. Tolstov, Galina A. Polyakova, Polina S. Bogdanova, Valentina A. Peterkova, Ivan I. Dedov |
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| Vol 62, No 1 (2016) |
ACTH ectopic syndrome caused by corticomedullary mixed tumor |
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Evgeniya Ivanovna Marova, Nikolay Sergeevich Kuznetsov, Lyudmila Yakovlevna Rozhinskaya, Oleg Valer'evich Remizov, Nonna Vadimovna Latkina, Ol'ga Vladimirovna Tikhonova, Lyubov Efimovna Kats, Iya Aleksandrovna Voronkova, Anastasiya Mikhaylovna Lapshina, Galina Sergeevna Kolesnikova |
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| Vol 62, No 1 (2016) |
The first clinical presentation of disorders of sex development 46 XY due to mutation in Steroidogenic factor 1 (SF1) in Russian Literature |
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Natalia Yur'evna Kalinchenko, Tatiana Aleksandrovna Anosova, Vitaliy Alekseevich Ioutsi, Anatoly Nikolaevich Tiulpakov |
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| Vol 61, No 6 (2015) |
Rare form of Permanent Neonatal Diabetes Mellitus (PNDM) due to novel mutation in EIF2AK3 gene (Wolcott—Rallison syndrome) |
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Yulia Viktorovna Tikhonovich, Olga Vasil'evna Stotikova, Petr Mikhaylovich Rubtsov, Anatoly Nikolaevich Tiulpakov |
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| Vol 55, No 2 (2009) |
Non-immune thyrotoxicosis caused by thyroid-stimulating hormone receptor activating gene mutation (the first description in Russia) |
Abstract
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V A Peterkova, O V Vasyukova, A N Tyul'pakov |
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| Vol 55, No 2 (2009) |
Clinical and molecular genetic verification of Frasers syndrome, false male hermaphroditism and chronic glomerulonephritis (the first description in Russia) |
Abstract
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E O Novikova, P M Rubtsov, P S Sverdlova, A N Tyul'pakov |
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| Vol 55, No 1 (2009) |
Surgery for thyroid cancer invading into the tracheal wall |
Abstract
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P. V. Svetitskiy |
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| Vol 55, No 1 (2009) |
The severe course of hyperparathyroidism in the elderly: Clinical cases |
Abstract
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N. G. Mokrysheva, S. S. Gulyaeva, L. Ya. Rozhinskaya, V. N. Smorshchok, M. A. Lysenko, N. S. Kuznetsov |
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| Vol 54, No 6 (2008) |
Severe hyperparathyroidism. Diagnostic difficulties (a description of a case) |
Abstract
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L G Strongin, V Ye Zagainov, K G Korneva, Ye A Yezhora, L Ye Berezova, M V Khazov, M Ye Nikitina, N Yu Orlinskaya, Yu V Shebasheva, N N Kushnikova |
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| Vol 54, No 6 (2008) |
Effect of human growth hormone on the status of collagen in the area of rat skin damage |
Abstract
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J Klebanovas, L Lasas, D Lasiene, V Barauskas |
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| Vol 54, No 4 (2008) |
The efficacy and safety of the insulin analogue de-temir (levemir): Clinical observation |
Abstract
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L. M. Sultanova, N. V. Krtnitskaya, Yu. V. Iskhakova, O. G. Pecheritsa |
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| Vol 54, No 3 (2008) |
Diuretic-induced edemas: Psychoendocrine aspects |
Abstract
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A. V. Dreval, Ye. G. Starostina, T. S. Kamynina, Yu. A. Kovaleva |
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| Vol 54, No 3 (2008) |
X-ray therapy for trophic skin changes in endogenous hypercorticism |
Abstract
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A. I. Bukhman, S. D. Arapova, N. L. Aglamazyan |
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| Vol 54, No 3 (2008) |
Thyroid papillary carcinoma in a patient with dyshormonal goiter |
Abstract
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A. Yu. Abrosimov, A. A. Ilyin |
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| Vol 53, No 4 (2007) |
Histiocytosis, central diabetes insipidus, and pregnancy |
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M. L. Kirilyuk, O. A. Slynko |
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| Vol 53, No 3 (2007) |
Follow-up of sisters, the enzygotic twins, with type 1 autoimmune polyglandular syndrome |
Abstract
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I. L. Nikitma |
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| Vol 53, No 3 (2007) |
Development of diffuse toxic goiter in the presence of prior hypothyroidism |
Abstract
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L. G. Strongm, K. G. Korneva, A. V. Petrov, E. A. Nekrasova, N. Z. Podupeiko, B. V. Sarantsev, N. Yu. Orlinskaya, N. I. Tarasova, Yu. V. Soldatova |
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| Vol 53, No 3 (2007) |
Pregnancy and labor in Turner's syndrome |
Abstract
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T. V. Vorobyeva, I. G. Torganova |
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| Vol 53, No 2 (2007) |
Hypothalamo-pituitary-adrenal axis disorders in diabetes |
Abstract
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N. K. Mazurina |
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| Vol 52, No 6 (2006) |
New mutation in the CYP17 gene: description of a case |
Abstract
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L. K. Dzeranova, A. N. Tyulpakov, Ye. A. Pigarova, P. M. Rubtsov, A. M. Artemova, A. V. Vorontsov, I. S. Yarovaya, L. Ya. Rozhinskaya, I. I. Dedov |
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| Vol 52, No 5 (2006) |
Type 1 polyglandular autoimmune syndrome 35 |
Abstract
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A Z Dreval, T S Kamynlna, O A Nechayeva, S S Tishenina A, Ye M Orlova |
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| Vol 52, No 4 (2006) |
Latent adrenal pheochromocytoma |
Abstract
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M В Babarina, K A Komshilova, V N Smorshok, N S Kuznetsov, L Ya Rozhlnskaya |
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| Vol 52, No 3 (2006) |
Itsenko-Cushing disease in the presence of testicular feminization syndrome |
Abstract
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L K Dzeranova, Ye N Giniyatullina, A A Pishchulin, I S Yarovaya, A N Tyulpakov |
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| Vol 52, No 3 (2006) |
Allgrow syndrome (triplet A) in a child endocrinologist's practice |
Abstract
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O A Maliyevsky, D S Nurmukhametova, V A Peterkova, Ye M Orlova, T V Semicheva, A Khebner |
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| Vol 52, No 3 (2006) |
Fasting hypogkycemia in a female patient without diabetes mellitus |
Abstract
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A Andrianov |
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| Vol 52, No 1 (2006) |
A case of olfactogenital dysplasia (Kallmann's syndrome) in females |
Abstract
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M. В. Babarina, A. V. Sekinayeva, Ye. N. Giniyatullina, L. Ya. Rozhinskaya |
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| Vol 51, No 5 (2005) |
The specific features of the course of acromegaly in old age and possibilities of somatulin treatment |
Abstract
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I. A. Ilovaiskaya, N N Molitvoslovova, A. V. Vorontsov, N. P. Goncharov, Ye. I. Marova |
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| Vol 51, No 1 (2005) |
Functional autonomy in endemic goiter |
Abstract
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N Yu Sviridenko |
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| Vol 50, No 6 (2004) |
Cushing's syndrome in a patient with medullary thyroid cancer glands |
Abstract
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N. V. Severskaya, A. A. Il'in, I. V. Chebotareva, P. A. Isaev, V. S. Medvedev, V. V. Popuchiev, P. O. Rumyantsev |
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| Vol 50, No 5 (2004) |
Three cases of mucoromycosis in patients with diabetes mellitus (Moscow region) |
Abstract
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A. V. Dreval', V. A. Gubkina, T. S. Kamynina, V. A. Loseva, E. V. Mel'nikova, V. G. Zenger, Z. M. Ashurov, V. M. Isaev, A. I. Sloeva, M. F. Makarenko, A. A. Ryabtseva, M. Yu. Luchkov, G. S. Kryuchkova |
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| Vol 50, No 3 (2004) |
Idiopathic hypoparathyroidism with epilepsy, optic atrophy and the syndrome of the "empty" Turkish saddle |
Abstract
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I. A. Bondar', V. V. Klimentov, L. D. Sorogina |
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| Vol 49, No 6 (2003) |
Q-infarction in a female patient with thyrotoxicosis |
Abstract
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G. P. Runov, N. N. Borovkov, Yu. V. Furmenkova |
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| Vol 49, No 4 (2003) |
Impaired sexual differentiation |
Abstract
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L. K. Dzeranova, I. S. Yarovaya, N. I. Sergeyeva, D. A. Derkach, Ye. I. Marova |
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