A. Tyulpakov

发表

[Familial partial lipodystrophy (Dunnigan syndrome) due to LMNA gene mutation: The first description of its clinical case in Russia].

G. Melnichenko, E. Sorkina, M. Kalashnikova, 2015, Terapevticheskii arkhiv.

Pituitary adenomas in the framework of hereditary syndromes

N. Mokrysheva, A. Tyulpakov, N. Mokrysheva, 2014 .

Ultrasonic predictors of macrosomia in gestational diabetes mellitus

M. A. Chechneva, N. Zubkova, A. Tyulpakov, 2019, Diabetes mellitus.

Fat tissue and adrenal function: mechanisms of mutual influence

A. Tyulpakov, E. Ershova, E. Troshina, 2019, Medical Council.

[CDC73 mutations in young patients with primary hyperparathyroidism: A description of two clinical cases].

Z. Belaya, V. Gorbunova, N. Mokrysheva, 2016, Terapevticheskii arkhiv.

[Kalmann syndrome in monozygous twins as an isolated manifestation of the SOX10 gene defect].

A. Tyulpakov, E. Vasilyev, O. Pilipenko, 2021, Problemy endokrinologii.

Mutations in transcription factor as rare causes of diabetes in pregnancy

N. Zubkova, A. Tyulpakov, E. Vasilyev, 2019, Diabetes mellitus.

Study of molecular basis of thyroid dysgenesis

A. Kolodkina, I. Dedov, A. Tyulpakov, 2018, Clinical and experimental thyroidology.

A clinical case of hereditary papillary thyroid carcinoma associated with a germline DICER 1 gene mutation ©

А. Н. Тюльпаков, A. Tyulpakov, P. Rumyantsev, 2017 .

Genotype-based personalized correction of glycemic control in patients with MODY due to mutations in GCK, HNF1A AND HNF4A genes

I. Dedov, N. Zubkova, A. Tyulpakov, 2017 .

Novel GLIS3 mutation in patient with neonatal diabetes mellitus and congenital hypothyroidism (NDH-syndrome)

А. Н. Тюльпаков, A. Tyulpakov, Y. Tikhonovich, 2022, Diabetes mellitus.

Osteogenesis imperfecta in combination with Graves disease

A. Tyulpakov, P. Rumiantsev, Румянцев Павел Олегович, 2017 .