Anatoly Tiulpakov
Overview
Explore the profile of Anatoly Tiulpakov including associated specialties, affiliations and a list of published articles.
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Articles
42
Citations
561
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Recent Articles
1.
Makretskaya N, Kalinchenko N, Tebieva I, Ionova S, Zinchenko R, Marakhonov A, et al.
Front Endocrinol (Lausanne)
. 2023 Jun;
14:1146768.
PMID: 37274334
Background: Congenital adrenal hyperplasia (CAH) caused by 3β-HSD deficiency is a rare form of congenital adrenal deficiency with an autosomal recessive type of inheritance. Previously we have demonstrated that a...
2.
Melikyan M, Gubaeva D, Shadrina A, Bolmasova A, Kareva M, Tiulpakov A, et al.
Front Endocrinol (Lausanne)
. 2023 May;
14:1127173.
PMID: 37152923
Background: Insulinomas are very rare in childhood with sparse knowledge on the clinical aspects and the presence of Multiple Endocrine Neoplasia type 1 (MEN1). Methods: We conducted a retrospective review...
3.
Oral E, Garg A, Tami J, Huang E, ODea L, Schmidt H, et al.
J Clin Lipidol
. 2022 Nov;
16(6):833-849.
PMID: 36402670
Background: Volanesorsen, an antisense oligonucleotide, is designed to inhibit hepatic apolipoprotein C-III synthesis and reduce plasma apolipoprotein C-III and triglyceride concentrations. Objective: The present study assessed efficacy and safety of...
4.
Aftab S, Gubaeva D, Houghton J, Dastamani A, Sotiridou E, Gilbert C, et al.
Endocr Connect
. 2022 Aug;
12(4).
PMID: 35951311
Background: Hyperinsulinism/hyperammonemia (HI/HA) syndrome is the second most common type of congenital hyperinsulinism caused by an activating GLUD1 mutation. Objective: The aim of this study was to determine the clinical...
5.
Viakhireva I, Kalinchenko N, Vasilyev E, Chistousova G, Filatova A, Marakhonov A, et al.
J Clin Endocrinol Metab
. 2022 Jul;
107(9):e3654-e3660.
PMID: 35775692
Context: The syndrome of adrenal insufficiency, obesity, and red hair is a rare autosomal recessive disorder. The majority of disease-causing variants associated with the syndrome are located in the coding...
6.
Tikhonovich Y, Petryaykina E, Zubkova N, Garyaeva I, Tiulpakov A
Acta Diabetol
. 2022 Jun;
59(9):1251-1253.
PMID: 35648253
No abstract available.
7.
Melikyan M, Gubaeva D, Nikitina I, Ryzhkova D, Mitrofanova L, Yukhacheva D, et al.
J Pediatr Endocrinol Metab
. 2021 Oct;
35(3):405-409.
PMID: 34700371
Objectives: Congenital hyperinsulinism (CHI) is a group of rare genetic disorders characterized by insulin overproduction. CHI causes life-threatening hypoglycemia in neonates and infants. Bloom syndrome is a rare autosomal recessive...
8.
Krupinova J, Mokrysheva N, Petrov V, Pigarova E, Eremkina A, Dobreva E, et al.
Endocrinol Diabetes Metab
. 2021 Sep;
4(4):e00284.
PMID: 34505413
Objective: To compare the serum miRNA expression profiles between patients with benign and malignant parathyroid tumours. Background: Despite recent advances in molecular biology, a histological tissue biopsy is still the...
9.
Mamedova E, Vasilyev E, Petrov V, Buryakina S, Tiulpakov A, Belaya Z
Front Endocrinol (Lausanne)
. 2021 Jun;
12:683492.
PMID: 34135865
Background: There are very few cases of co-occurring pituitary adenoma (PA) and pheochromocytomas (PCC)/paragangliomas caused by mutations. No cases of familial PA in patients with mutations have been described to...
10.
Yukina M, Nuralieva N, Sorkina E, Troshina E, Tiulpakov A, Belaya Z, et al.
Endocrinol Diabetes Metab Case Rep
. 2021 Apr;
2021.
PMID: 33859056
Summary: Lamin A/C (LMNA) gene mutations cause a heterogeneous group of progeroid disorders, including Hutchinson-Gilford progeria syndrome, mandibuloacral dysplasia, atypical progeroid syndrome (APS) and generalized lipodystrophy-associated progeroid syndrome (GLPS). All...