Results 11 to 20 of about 2,561,602 (268)

Necrotising pancreatitis in a patient with CREST syndrome: a rare autoimmune gastrointestinal complication [PDF]

European Journal of Case Reports in Internal Medicine
Necrotising pancreatitis is a severe and life-threatening form of acute pancreatitis characterised by the necrosis of pancreatic and peripancreatic tissues due to intense inflammation and autodigestion.
Antonio Al Hazzouri, Philippe Attieh, George Ghaleb, Ahmad Khalil, Noura Chamchoum, Karam Karam, Elias Fiani   +6 more
doaj   +2 more sources

Long-term outcomes in patients with primary biliary cholangitis complicated with CREST syndrome [PDF]

Scientific Reports
Primary biliary cholangitis (PBC) is frequently associated with autoimmune disease. Although PBC complicated with CREST syndrome (PBC-CREST) has been reported, the long-term outcomes of the affected patients have not been fully investigated.
Kazumichi Abe, Manabu Hayashi, Tatsuro Sugaya, Naoto Abe, Yosuke Takahata, Masashi Fujita, Atsushi Takahashi, Kiyoshi Migita, Hiromasa Ohira   +8 more
doaj   +2 more sources

CREST syndrome

Skinmed, 2018
Piyush, Kumar, Anupam, Das
semanticscholar   +4 more sources

Cardio-cephalic neural crest syndrome: A novel hypothesis of vascular neurocristopathy. [PDF]

Interv Neuroradiol, 2017
Komiyama M.
europepmc   +2 more sources

Severe Spinal Stenosis Secondary to a CREST Syndrome Related Calcific Deposit: A Case Report [PDF]

Spine Surgery and Related Research
Henry Howard, Michael Newman, Henry Budd
doaj   +2 more sources

Shared reproductive disruption, not neural crest or tameness, explains the domestication syndrome

Proceedings of the Royal Society B, 2023
Altered neural crest cell (NCC) behaviour is an increasingly cited explanation for the domestication syndrome in animals. However, recent authors have questioned this explanation, while others cast doubt on whether domestication syndrome even exists ...
B. Gleeson, L. Wilson
semanticscholar   +1 more source

MAPRE2 mutations result in altered human cranial neural crest migration, underlying craniofacial malformations in CSC-KT syndrome

Scientific Reports, 2021
Circumferential skin creases (CSC-KT) is a rare polymalformative syndrome characterised by intellectual disability associated with skin creases on the limbs, and very characteristic craniofacial malformations.
Cedric Thues, J. S. Valadas, Liesbeth Deaulmerie, Ann Geens, Amit K. Chouhan, Ramon Duran-Romaña, J. Schymkowitz, F. Rousseau, Michaela Bartusel, Rizwan Rehimi, Á. Rada-Iglesias, P. Verstreken, H. Van Esch   +12 more
semanticscholar   +1 more source

Adenocarcinoma of the third portion of the duodenum in a man with CREST syndrome

World Journal of Surgical Oncology, 2008
Background CREST (Calcinosis, Raynaud's phenomenon, Esophageal dysmotility, Sclerodactyly and Telangiectasias) syndrome has been rarely associated with other malignancies (lung, esophagus).This is the first report of a primary adenocarcinoma of the third
Fragulidis Georgios, Theodosopoulos Theodosios, Konstantinidis Christos, Marinis Athanasios, Anastasopoulos Georgios, Vassiliou Ioannis   +5 more
doaj   +1 more source

CHARGE syndrome modeling using patient-iPSCs reveals defective migration of neural crest cells harboring CHD7 mutations

eLife, 2017
CHARGE syndrome is caused by heterozygous mutations in the chromatin remodeler, CHD7, and is characterized by a set of malformations that, on clinical grounds, were historically postulated to arise from defects in neural crest formation during ...
Hironobu Okuno, Francois Renault Mihara, Shigeki Ohta, Kimiko Fukuda, Kenji Kurosawa, Wado Akamatsu, Tsukasa Sanosaka, Jun Kohyama, Kanehiro Hayashi, Kazunori Nakajima, Takao Takahashi, Joanna Wysocka, Kenjiro Kosaki, Hideyuki Okano   +13 more
doaj   +1 more source

The Core Splicing Factors EFTUD2, SNRPB and TXNL4A Are Essential for Neural Crest and Craniofacial Development

Journal of Developmental Biology, 2022
Mandibulofacial dysostosis (MFD) is a human congenital disorder characterized by hypoplastic neural-crest-derived craniofacial bones often associated with outer and middle ear defects.
Byung-Yong Park, Melanie Tachi-Duprat, Chibuike Ihewulezi, Arun Devotta, Jean-Pierre Saint-Jeannet   +4 more
doaj   +1 more source