Results 21 to 30 of about 7,139 (182)

Syndromic (phenotypic) diarrhea in early infancy

Orphanet Journal of Rare Diseases, 2008
Syndromic diarrhea (SD), also known as phenotypic diarrhea (PD) or tricho-hepato-enteric syndrome (THE), is a congenital enteropathy presenting with early-onset of severe diarrhea requiring parenteral nutrition (PN).
Bodemer Christine, Brousse Nicole, Roquelaure Bertrand, Vinson Christine, Goulet Olivier, Cézard Jean-Pierre   +5 more
doaj   +1 more source

Apoptotic colopathy following bendamustine therapy

Human Pathology Reports, 2023
A 60-year-old woman with marginal zone lymphoma was treated with obinutuzumab and bendamustine after failing rituximab. She later developed intractable nausea and diarrhea which resulted in a dramatic weight loss and multiple hospitalizations. During her
Vincent Czerwinski, Wei Cui, Marc Hoffmann   +2 more
doaj   +1 more source

Tufting Enteropathy: A Review of Clinical and Histological Presentation, Etiology, Management, and Outcome

Gastroenterology Research and Practice, 2020
Congenital tufting enteropathy (CTE), also named intestinal epithelial dysplasia, is a rare, autosomal recessive enteropathy with persistent and life-threatening intractable diarrhea early in life. Intractable diarrhea is present independent of breast or
Changzhou Cai, Yishu Chen, Xueyang Chen, Feng Ji   +3 more
doaj   +1 more source

Trichohepatoenteric Syndrome or Syndromic Diarrhea—Report of Three Members in a Family, First Report from Iran

Case Reports in Pathology, 2016
Introduction. Intractable diarrhea of infancy (IDI) includes several types of early onset diarrhea; one of the rare etiologies is trichohepatoenteric (THE) syndrome, also known as syndromic diarrhea (SD) which was primarily described by Stankler et al ...
F. E. Mahjoub, F. Imanzadeh, S. Mahdavi Izadi, A. Nahali Moghaddam   +3 more
doaj   +1 more source

Carbamazepine-Induced Diarrhea

Pediatric Neurology Briefs, 1992
Intractable diarrhea induced by carbamazepine (CBZ) in 3 patients and necessitating discontinuation of the drug is reported from the Departments of Neurology and Medicine, University of Louisville School of Medicine, Kentucky.
J Gordon Millichap
doaj   +1 more source

Syndromic diarrhea/Tricho-hepato-enteric syndrome

Orphanet Journal of Rare Diseases, 2013
Syndromic diarrhea/Tricho-hepato-enteric syndrome (SD/THE) is a rare and severe bowel disorder caused by mutation in SKIV2L or in TTC37, 2 genes encoding subunits of the putative human SKI complex.
Fabre Alexandre, Martinez-Vinson Christine, Goulet Olivier, Badens Catherine   +3 more
doaj   +1 more source

DRIVE‐SAFE: Data‐Driven Robustness and Informed Validation for Evolving Specifications via Formal Evaluation

Advanced Robotics Research, EarlyView.
DRIVE‐SAFE evaluates learning‐based, black‐box autonomous driving policies against evolving temporal safety requirements using Signal Temporal Logic robustness metrics. It aggregates distributional robustness measures with domain‐informed weights to guide iterative retraining.
Kristy Sakano, Jianyu An, Dinesh Manocha, Huan Xu   +3 more
wiley   +1 more source

“Intrapericardial Approach” for Venous Outflow Reconstruction in Living‐Donor Liver Transplantation for Budd‐Chiari Syndrome: Surgical Techniques and LongTerm Outcomes

Annals of Gastroenterological Surgery, EarlyView.
Unlike deceased‐donor liver transplantation, living‐donor liver transplantation (LDLT) for Budd‐Chiari Syndrome (BCS) presents distinctive challenges in hepatic venous (HV)‐outflow reconstruction because diseased HV–inferior vena cava (IVC) cannot be entirely replaced with healthy donor vessels.
Koichiro Hata, Tetsuya Tajima, Satoshi Ogiso, Shinji Uemoto, Etsuro Hatano   +4 more
wiley   +1 more source

Unusual feature of neonatal hypernatremic dehydration due to microvillus inclusion disease: a case report

The Pan African Medical Journal, 2018
All over the causes of intractable diarrhea of infancy, microvillous inclusion disease is a rare congenital defect of intestinal brush border of unknown aetiology.
Fatma Khalsi, Mohamed Riadh Boukhris, Ines Brini, Jean Pierre Hugot, Patsy Dominique Berrebi, Khedija Boussetta   +5 more
doaj   +1 more source

Interpretability and Representability of Commutative Algebra, Algebraic Topology, and Topological Spectral Theory for Real‐World Data

Advanced Intelligent Discovery, EarlyView.
This article investigates how persistent homology, persistent Laplacians, and persistent commutative algebra reveal complementary geometric, topological, and algebraic invariants or signatures of real‐world data. By analyzing shapes, synthetic complexes, fullerenes, and biomolecules, the article shows how these mathematical frameworks enhance ...
Yiming Ren, Guo‐Wei Wei
wiley   +1 more source