نتایج جستجو برای: mowat syndrome

تعداد نتایج: 621961  

Journal: :Seizure 2010
Marianna Pezzella Nune S. Yeghiazaryan Pierangelo Veggiotti Alberto Bettinelli Giovanna Giudizioso Federico Zara Pasquale Striano Carlo Minetti

Galloway-Mowat Syndrome (GMS) is an autosomal recessively inherited condition which manifests with severe encephalopathy, featuring microcephaly, developmental delay, and early-onset intractable epilepsy. Patients typically show also renal involvement from the onset. We report two siblings with GMS presenting with early-onset, intractable epilepsy and neurological deterioration, later followed ...

Journal: :Developmental biology 2010
Laure Stanchina Tom Van de Putte Michel Goossens Danny Huylebroeck Nadege Bondurand

The involvement of SOX10 and ZFHX1B in Waardenburg-Hirschsprung disease (hypopigmentation, deafness, and absence of enteric ganglia) and Mowat-Wilson syndrome (mental retardation, facial dysmorphy and variable congenital malformations including Hirschsprung disease) respectively, highlighted the importance of both transcription factors during enteric nervous system (ENS) development. The expres...

2011
Daniel B. McClatchy Lujian Liao Sung Kyu Park Tao Xu Bingwen Lu John R. Yates III

Differential expression of proteins between tissues underlies organ-specific functions. Under certain pathological conditions, this may also lead to tissue vulnerability. Furthermore, post-translational modifications exist between different cell types and pathological conditions. We employed SILAM (Stable Isotope Labeling in Mammals) combined with mass spectrometry to quantify the proteome betw...

پایان نامه :وزارت بهداشت، درمان و آموزش پزشکی - دانشگاه علوم پزشکی و خدمات بهداشتی درمانی استان فارس - دانشکده دندانپزشکی 1399

چکیده ندارد.

Journal: :Partnership: The Canadian Journal of Library and Information Practice and Research 2008

2017
Marcella Zollino Serena Lattante Daniela Orteschi Silvia Frangella Paolo N. Doronzio Ilaria Contaldo Eugenio Mercuri Giuseppe Marangi

Craniosynostosis is a heterogeneous condition caused by the premature fusion of cranial sutures, occurring mostly as an isolated anomaly. Pathogenesis of non-syndromic forms of craniosynostosis is largely unknown. In about 15-30% of cases craniosynostosis occurs in association with other physical anomalies and it is referred to as syndromic craniosynostosis. Syndromic forms of craniosynostosis ...

2014
Dorien Baetens Wilhelm Mladenov Barbara Delle Chiaie Björn Menten An Desloovere Violeta Iotova Bert Callewaert Erik Van Laecke Piet Hoebeke Elfride De Baere Martine Cools

BACKGROUND One in 4500 children is born with ambiguous genitalia, milder phenotypes occur in one in 300 newborns. Conventional time-consuming hormonal and genetic work-up provides a genetic diagnosis in around 20-40% of 46,XY cases with ambiguous genitalia. All others remain without a definitive diagnosis. The investigation of milder cases, as suggested by recent reports remains controversial. ...

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