Search Results - "Tiulpakov"

Author index.

Source: Andrology. Sep2024 Supplement 1, Vol. 12, p149-156. 8p.

Genetically Confirmed Osteogenesis Imperfecta (COL1A1) With Unexplained Ambiguous Genitalia in a 46,XY Child: An Index Case Report.

Authors: Agarwal, Harshita Jha, Tathagata Azmi, Mohammad Orooj et al.

Source: Clinical Case Reports. Jul2026, Vol. 14 Issue 7, p1-6. 6p.

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Aromatase excess syndrome in children: insight on pathophysiology, clinical manifestation, and management.

Authors: Metwalley, Kotb Abbass Farghaly, Hekma Saad

Source: Journal of Rare Diseases. 2/12/2026, Vol. 5 Issue 1, p1-7. 7p.

Functional Properties of POU1F1 Mutants in the Transcriptional Regulation of the Thyrotropin β Gene Compared with the Prolactin Gene.

Authors: Kawauchi, Yuto Sasaki, Shigekazu Matsushita, Akio et al.

Source: International Journal of Molecular Sciences. Jan2026, Vol. 27 Issue 1, p119. 22p.

Bimodal Genomic Approach Predicting Semaphorin 7A (SEMA7A) as Prognostic Biomarker in Adrenocortical Carcinoma.

Authors: Dhall, Anjali Taniyama, Daiki Elloumi, Fathi et al.

Source: Cancers. Jul2025, Vol. 17 Issue 13, p2078. 16p.

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Differentiation of Human Pluripotent Cells into Pancreatic Beta Cells for Disease Modeling and Cell Replacement Therapy for Diabetes.

Authors: Barinova, Anna A. Bogomolova, Alexandra Y. Bogomazova, Alexandra N. et al.

Source: International Journal of Molecular Sciences. Sep2025, Vol. 26 Issue 17, p8749. 15p.

Raman Spectroscopic Analysis of Molecular Structure and Mechanical Properties of Hypophosphatasia Primary Tooth.

Authors: Imamura, Hayata Adachi, Tetsuya Zhu, Wenliang et al.

Source: Molecules. Dec2024, Vol. 29 Issue 24, p6049. 16p.

Clean intermittent catheterization reverses hydronephrosis in a child with congenital nephrogenic diabetes insipidus: a case report.

Authors: Xie J Wu J Zhang Q et al.

Source: The Canadian journal of urology [Can J Urol] 2026 Jun 26; Vol. 33 (3), pp. 723-728. Date of Electronic Publication: 2026 Jun 26.

Publication Type: Case Reports; Journal Article

Journal Info: Publisher: CJU Communications Country of Publication: United States NLM ID: 9515842 Publication Model: Electronic Cited Medium: Internet ISSN: 1488-5581 (Electronic) Linking ISSN: 11959479 NLM ISO Abbreviation: Can J Urol Subsets: MEDLINE

High carrier frequency of a nonsense p.Trp230* variant in HSD3B2 gene in Ossetians.

Authors: Makretskaya N Kalinchenko N Tebieva I et al.

Source: Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2023 May 16; Vol. 14, pp. 1146768. Date of Electronic Publication: 2023 May 16 (Print Publication: 2023).

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101555782 Publication Model: eCollection Cited Medium: Print ISSN: 1664-2392 (Print) Linking ISSN: 16642392 NLM ISO Abbreviation: Front Endocrinol (Lausanne) Subsets: MEDLINE

Insulinoma in childhood: a retrospective review of 22 patients from one referral centre.

Authors: Melikyan M Gubaeva D Shadrina A et al.

Source: Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2023 Apr 19; Vol. 14, pp. 1127173. Date of Electronic Publication: 2023 Apr 19 (Print Publication: 2023).

Publication Type: Journal Article

Journal Info: Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101555782 Publication Model: eCollection Cited Medium: Print ISSN: 1664-2392 (Print) Linking ISSN: 16642392 NLM ISO Abbreviation: Front Endocrinol (Lausanne) Subsets: MEDLINE

Parathyroid Carcinoma: From Molecular Pathogenesis and Diagnostic Biomarkers to Targeted Therapeutics.

Authors: Wang, Chunlong Wu, Xiaoqing Liu, Yuqin

Source: International Journal of Molecular Sciences. May2026, Vol. 27 Issue 10, p4549. 15p.

Current and Emerging Pharmacological Therapies for Hypertriglyceridemia.

Authors: Alhomoud, Ibrahim S.¹ (AUTHOR)

Source: International Journal of Molecular Sciences. Apr2026, Vol. 27 Issue 8, p3573. 20p.

A novel detrimental homozygous mutation in the WFS1 gene in two sisters from nonconsanguineous parents with untreated diabetes insipidus.

Authors: Papadimitriou, Dimitrios T. Kleanthous, Kleanthis Manolakos, Emmanouil et al.

Source: Clinical Case Reports. Dec2019, Vol. 7 Issue 12, p2355-2357. 3p.

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LEMD2‐associated progeroid syndrome: Expanding the phenotype of the nuclear envelopathy caused by a defect in LEMD2 gene.

Authors: Matter, Alyssia Kaufman, Christina Zürcher, Nadia et al.

Source: Aging Cell. Aug2024, Vol. 23 Issue 8, p1-7. 7p.

Identification of POU1F1 Variants in Vietnamese Patients with Combined Pituitary Hormone Deficiency.

Authors: Nguyen, Ha Thu Nguyen, Khanh Ngoc Dien, Tran Minh et al.

Source: International Journal of Molecular Sciences. Mar2025, Vol. 26 Issue 6, p2406. 14p.

Growth Without GH: A Case Series and Literature Review.

Authors: Bilha, Stefana Catalina Preda, Cristina Leustean, Letitia et al.

Source: Journal of Clinical Medicine. Dec2025, Vol. 14 Issue 24, p8957. 19p.