Results 171 to 180 of about 118,339 (295)

Regulation of heme oxygenase-1 induction during recurrent insulin induced hypoglycemia

, 2014
Syed Quadri, Priyanka Prathipati, Debra Jackson, Keith E. Jackson   +3 more
openalex   +2 more sources

Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death [PDF]

, 2001
Jamal A. Ibdah, Hyacinth Paul, Yiwen Zhao, Scott Binford, Ken Salleng, Mark A. Cline, Dietrich Matern, Michael J. Bennett, Piero Rinaldo, Arnold W. Strauss   +9 more
openalex   +1 more source

Esophageal stenosis secondary to severe loxoscelism: A case report

JPGN Reports, EarlyView.
ABSTRACT Loxoscelism is a public health issue in tropical countries, particularly in Brazil. It can affect children of all ages and may lead to severe and irreversible injuries. We report the case of an infant who suffered a severe loxoscelism accident in the cervical region, progressing to esophageal stricture requiring multiple dilations. Fortunately,
Lucas Rocha Alvarenga, Mariana Di Paula Rodrigues, Marise Helena Cardoso Tofoli, Patrícia dos Santos Oliveira   +3 more
wiley   +1 more source

Accurate prediction of hypoglycemia and hyperglycemia using machine learning in critically ill patients. [PDF]

Sci Rep
Ikeda Y, Sugimoto S, Ishikawa T, Yokoyama T, Oami T, Tomita K, Kawakami E, Nakada TA.   +7 more
europepmc   +1 more source

Interoceptive Awareness Is Associated With Impaired Awareness of Hypoglycemia in Adults With Type 1 Diabetes [PDF]

Austin Matus, Bárbara Riegel, Michael R. Rickels   +2 more
openalex   +1 more source

Improved Prandial Glucose Control With Lower Risk of Hypoglycemia With Nateglinide Than With Glibenclamide in Patients With Maturity-Onset Diabetes of the Young Type 3 [PDF]

, 2006
Jaakko Tuomilehto, Elina H. Honkanen, Bo Isomaa, Leena Sarelin, Leif Groop   +4 more
openalex   +1 more source

Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea

JPGN Reports, EarlyView.
Abstract Among congenital diarrhea and enteropathies (CODEs), proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency is a rare monogenic disorder, associated with severe neonatal diarrhea and polyendocrinopathies. We report an 18‐day‐old male neonate, born to consanguineous parents, presenting with persistent watery diarrhea, metabolic ...
Eleonora Saraceno, Angelo Corso Faini, Silvia Deaglio, Marianna Pellegrini, Raffaele Buganza, Francesca Giuliani, Pier Luigi Calvo, Michele Pinon   +7 more
wiley   +1 more source

13. Older Adults: Standards of Care in Diabetes-2026. [PDF]

Diabetes Care
American Diabetes Association Professional Practice Committee for Diabetes* .
europepmc   +1 more source

The selfish yet forgetful brain: Stable cerebral oxygen metabolism during hypoglycemia but impaired memory consolidation [PDF]

Antonia Bose, Stefanie J. Haschka, Johanna Koehler, Felix Hesse, Bruce Martin, Lea Steinberg, Roman Iakoubov, Valentin Riedl   +7 more
openalex   +1 more source

Long Term Metabolic Outcomes Following Pancreatectomy and Autologous Islet Transplantation: Systematic Review and Meta‐Analysis

Journal of Surgical Oncology, EarlyView.
ABSTRACT This systematic review and meta‐analysis assessed long‐term outcomes following total pancreatectomy with islet autotransplantation (TPIAT). Seventeen studies including 1332 patients were analyzed. The pooled insulin independence rate was 34%, with higher rates for non‐chronic pancreatitis indications (68%) versus chronic pancreatitis (33 ...
Daniel L. Hughes, Caterina Di Bella, Benedetta Quaratino, Pietro Rigo, Giulia Cirillo, Gioia Sgrinzato, Umberto Cillo, Lucrezia Furian, Giovanni Marchegiani   +8 more
wiley   +1 more source