Results 191 to 200 of about 119,841 (316)

Vitamin B12 deficiency in a pediatric patient with gastric obstruction and jejunal feeding dependence: A case report

JPGN Reports, EarlyView.
Abstract Pediatric B12 deficiency is most caused by insufficient dietary intake, malabsorption or autoimmune gastritis. We present a unique case of B12 deficiency in a pediatric patient with complex gastrointestinal anatomy and jejunal nutritional dependence nearly two decades after unsuccessful surgical intervention.
Angela H. Nguyen, Dorsey Bass, Rachel E. Herdes   +2 more
wiley   +1 more source

Thyroid Hormones Regulate Postprandial Glucose Metabolism by Regulating SGLT1 Expression in the Small Intestine in Rats and Mice. [PDF]

Int J Mol Sci
Matsumoto S, Yoshino S, Okada S, Horiguchi K, Hashimoto K, Yamada E.   +5 more
europepmc   +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

Association of ambient air pollutants with maternal thyroid hormones during the entire pregnancy. [PDF]

Sci Rep
Guo F, Pan X, Gu S, Xu Q, Duan J, Wang X, Chen Z, Fu Q, Mao G, Xu P, Xu D, Huang X, Li Y, Jiang Y, Liu C, Mo Z.   +15 more
europepmc   +1 more source

Gastrointestinal strictures in a pediatric patient with Satoyoshi syndrome

JPGN Reports, EarlyView.
Abstract We present a novel case of gastrointestinal strictures in a young girl with Satoyoshi syndrome (SS), highlighting multi‐system features of alopecia universalis, painful muscle cramps with dystonia, aberrant growth velocity, and skeletal abnormalities.
Katherine (Tusia) Pohoreski, Gary Galante, Kiera Pajunen, Marie‐Anne Brundler, Samarjeet Bhandal, Iwona Wrobel   +5 more
wiley   +1 more source

Exploring the relationships between clinical manifestations and sex hormones, thyroid hormones, and menstrual factors in female Parkinson's disease patients. [PDF]

Front Med (Lausanne)
Wang F, Zhao J, Du J, Li J, Wang P, Yi Z, Feng T, Wan Z.   +7 more
europepmc   +1 more source

Menetrier's: A pediatric chronic state of disease with a possible heritable form

JPGN Reports, EarlyView.
Abstract Menetrier's disease (MD) is a rare, typically transient, hypertrophic gastropathy with under 1000 adult cases and 50 pediatric cases known worldwide. Pediatric cases most often present with an infectious etiology. We present a case of a teenage male expressing a chronic state of disease without infectious origin.
MariaElena Terzis, Anna Furr, Julia Fritz   +2 more
wiley   +1 more source

Quantitative Analysis of Selected Circulating Hematological Biomarkers, Essential Minerals, Vitamins, and Thyroid Hormones in Females Affected by Hair Loss. [PDF]

Diseases
Al-Fawaeir S, Al-Odat I.
europepmc   +1 more source

Trisomy 21 Disrupts Thyroid Hormones Signaling During Human iPSC-Derived Neural Differentiation In Vitro. [PDF]

Cells
de Souza JS, Sanchez-Sanchez S, Amelinez-Robles N, Guerra BS, Giannocco G, Muotri AR.   +5 more
europepmc   +1 more source

Analysis of ligand-dependent changes in estrogen receptor and thyroid hormone receptor mRNA and protein expression in the developing rat cerebellum [PDF]

, 2011
Attila Zsarnovszky, István Tóth, Trudy Scalise Johnson, Virág Somogyi, Andrea Győrffy, Dávid Sándor Kiss, Gréta Goszleth, Tibor Bartha, Vilmos László Frenyó   +8 more
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