Results 111 to 120 of about 8,944 (181)

Case Report: Pasireotide treatment in neonatal congenital hyperinsulinism due to a homozygous <i>ABCC8</i> mutation. [PDF]

Front Endocrinol (Lausanne)
Kurz C, Roeper M, Friesl L, Mayatepek E, Meissner T, Kummer S, Hoermann H, Welters A.   +7 more
europepmc   +1 more source

Two threats in early life: congenital hyperinsulinemic hypoglycemia and thrombosis. [PDF]

Ther Adv Endocrinol Metab
Turktan I, Çetin SK, Senyazar G, Karaca SE, Abseyi SN, Demirtas S, Ozsu E, Aycan Z, Berberoglu M, Siklar Z.   +9 more
europepmc   +1 more source

Post-bariatric hypoglycaemia: from altered gut physiology to targeted therapies. [PDF]

Endocr Connect
Yang W, Tan TM.
europepmc   +1 more source

Determinants of hyperinsulinism severity in children with Beckwith-Wiedemann syndrome.

J Clin Endocrinol Metab
George AM, Viswanathan A, Sussman JH, Hathaway ER, Casalnova A, Nesbitt S, Boodhansingh KE, Stewart NM, McKnight HJ, Lord K, De León DD, Stanley CA, Adzick NS, Ganguly A, Kalish JM.   +14 more
europepmc   +1 more source

Leveraging bioinformatics approaches for drug repositioning in space radiation protection. [PDF]

PLoS One
Diaz TE, Kerrigan JA, Bowles DE, Kidane YH.   +3 more
europepmc   +1 more source

A case of congenital hyperinsulinism with <i>ABCC8</i> variants treated with octreotide long-acting release for four years. [PDF]

Clin Pediatr Endocrinol
Umeki I, Nakagawa T, Miura A, Kawashima S, Shima H, Sogi C, Suzuki D, Ito M, Ishibashi N, Suzuki S, Takahashi T, Yorifuji T, Kikuchi A, Kanno J.   +13 more
europepmc   +1 more source

Erratum: A Review of Current Trends with Type 2 Diabetes Epidemiology, Aetiology, Pathogenesis, Treatments and Future Perspectives [Corrigendum]. [PDF]

Diabetes Metab Syndr Obes
europepmc   +1 more source

Vykat XR (diazoxide choline-extended release): a new FDA-approved treatment for hyperphagia in Prader-Willi syndrome. [PDF]

Ann Med Surg (Lond)
Pokhrel P, Noorul HS, Fatima L, Kumar A, Samad AA, Ferrer GF.   +5 more
europepmc   +1 more source

Antenatal management of <i>HNF4A</i>-MODY and <i>INSR</i> mutations in pregnancy. [PDF]

JCEM Case Rep
Wu K, Russell H, Rodrigo N.
europepmc   +1 more source