Results 201 to 210 of about 196,449 (311)

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 surgery outcomes in a 4-year series with intraoperative neuromonitoring: a retrospective cohort study. [PDF]

Gland Surg
Allen M, Palma C, Branco C, Resende C, Vieira N, Silva AL, Sobral do Rosário F.   +6 more
europepmc   +1 more source

Recent Advances in Thyroid Surgery

Sudharsanan Sundaramurthi, Sandeep Dabhekar   +1 more
openalex   +2 more sources

Autoantibody signatures in children with celiac disease, juvenile idiopathic arthritis, and polyautoimmunity

JPGN Reports, EarlyView.
Abstract Objective To determine if multiplex autoantibody arrays can identify novel biomarker signatures in children with one or multiple autoimmune diseases (polyautoimmunity). Methods Plasma collected from children (18 years or younger) in the Boston Children's Hospital Precision Link Biobank for Health Discovery between January 2007 and June 2021 ...
Nan Du, Denis Chang, Madison Wong, Jay R. Thiagarajah, Erin Janssen, Lauren A. Henderson, Krishnan Raghunathan, Jocelyn A. Silvester   +7 more
wiley   +1 more source

‌Refined supraclavicular approach in unilateral thyroid surgery: balancing minimal invasion with oncologic radicality‌. [PDF]

BMC Surg
Wang J, Luo J, Fu W, Wei M, Dai Y.
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

Platycodon grandiflorum Extract Alleviates Inflammation During Asthma Development In Vivo and In Vitro

Analytical Cellular Pathology
Jie Liu, Wei Li, Jingchao Yu, Jinle Lu, Yanan Wei   +4 more
doaj   +1 more source

Horner syndrome following endoscopic thyroid surgery (ETS): a report of two cases and literature review. [PDF]

Front Med (Lausanne)
Xie TH, Fu Y, Jin XS, Ha SN, Ren XX, Sun XL, Niu Z.   +6 more
europepmc   +1 more source

Hepatopulmonary syndrome as presentation of pediatric metabolic dysfunction‐associated steatohepatitis

JPGN Reports, EarlyView.
Abstract Childhood obesity is rising and leading to serious co‐morbidities, among which is metabolic dysfunction‐associated steatotic liver disease (MASLD) predisposing individuals to cirrhosis. We describe a young 11‐year‐old Hispanic male who presented with hepatopulmonary syndrome secondary to cirrhotic portal hypertension from metabolic dysfunction‐
Shruti Sakhuja, Stacey S. Beer, Kalyani R. Patel, Alexiss M. Williams, Nhu Thao Galvan, John A. Goss, Krupa R. Mysore   +6 more
wiley   +1 more source