Results 151 to 160 of about 14,238 (246)

Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism [PDF]

, 2005
Mariko Suchi, Courtney MacMullen, Paul Thornton, N. Scott Adzick, Arupa Ganguly, Eduardo D. Ruchelli, Charles A. Stanley   +6 more
openalex   +1 more source

Neonatal Cholestasis Associated With Transient Congenital Hyperinsulinism: A Case Report. [PDF]

Cureus
Ibi K, Shitara Y, Adachi N, Tanaka H, Takahashi N.   +4 more
europepmc   +1 more source

A Novel KCNJ11 Mutation Associated with Congenital Hyperinsulinism Reduces the Intrinsic Open Probability of β-Cell ATP-sensitive Potassium Channels [PDF]

, 2005
Yu-Wen Lin, Courtney MacMullen, Arupa Ganguly, Charles A. Stanley, Show‐Ling Shyng   +4 more
openalex   +1 more source

Serum Glucagon Counterregulatory Hormonal Response to Hypoglycemia Is Blunted in Congenital Hyperinsulinism [PDF]

, 2005
Khalid Hussain, Joseph Bryan, Henrik Thybo Christesen, Klaus Brusgaard, Lydia Aguilar‐Bryan   +4 more
openalex   +1 more source

Large copy number variants are an important cause of congenital hyperinsulinism that should be screened for during routine testing. [PDF]

Front Endocrinol (Lausanne)
Flanagan SE, Lazaridi IA, Männistö JME, Bennett JJ, Kalyon O, Johnson MB, Wakeling MN, Houghton JAL, Laver TW.   +8 more
europepmc   +1 more source

Postprandial Hypoglycemia in a Patient With Clinical Beckwith-Wiedemann Syndrome. [PDF]

JCEM Case Rep
London B, Corker LC, Deng L, Mani B, Murray A, Krishnamurthy M.   +5 more
europepmc   +1 more source

Sensitization to Insulin in Adolescent Girls to Normalize Hirsutism, Hyperandrogenism, Oligomenorrhea, Dyslipidemia, and Hyperinsulinism after Precocious Pubarche

, 2001
Ajuah Davis
openalex   +1 more source

The Knudson’s Two-Hit Model and Timing of Somatic Mutation May Account for the Phenotypic Diversity of Focal Congenital Hyperinsulinism [PDF]

, 2006
Irina Giurgea, Christine Sempoux, Christine Bellanné‐Chantelot, Maria João Ribeiro, Laurence Hubert, Nathalie Boddaert, Jean‐Marie Saudubray, Jean‐Jacques Robert, Françis Brunelle, Jacques Rahier, Francis Jaubert, Claire Nihoul‐Feketé, Pascale de Lonlay   +12 more
openalex   +1 more source

A Japanese Case of Congenital Hyperinsulinism with Hyperammonemia Due to a Mutation in Glutamate Dehydrogenase (GLUD1) Gene.

, 2001
Kazuki Yasuda, Naoya Koda, Hiroko Kadowaki, Yoshihiro Ogawa, Satoshi Kimura, Takashi Kadowaki, Yasuo Akanuma   +6 more
openalex   +2 more sources

Congenital Hyperinsulinism–Associated ABCC8 Mutations That Cause Defective Trafficking of ATP-Sensitive K+ Channels [PDF]

, 2007
Fei-Fei Yan, Yu-Wen Lin, Courtney MacMullen, Arupa Ganguly, Charles A. Stanley, Show‐Ling Shyng   +5 more
openalex   +1 more source