نتایج جستجو برای: harlequin fetus

تعداد نتایج: 26697  

2016
Kruti Parikh Kanwaljit Brar Jaimie B. Glick Alexandra Flamm Sharon A. Glick

ABCA12: adenosine triphosphate binding cassette A12 HI: harlequin ichthyosis NICU: neonatal intensive care unit INTRODUCTION Harlequin ichthyosis (HI) is a rare autosomal recessive congenital ichthyosis associated with mutations in the keratinocyte lipid transporter adenosine triphosphate binding cassette A12 (ABCA12), leading to disruption in lipid and protease transport into lamellar granules...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1997
D A Morrison K Bibby G Woodruff

When trying to establish the likely anatomical site (preganglionic or postganglionic) of a lesion causing congenital Horner's syndrome, the distribution of facial flushing (the "harlequin" sign), may be seen. In babies and young children, facial flushing is a relatively simple clinical sign to demonstrate, compared with facial sweating. In unilateral facial flushing the areas that do not flush ...

2017
Paule Bénit Alice Pelhaître Elise Saunier Sylvie Bortoli Assetou Coulibaly Malgorzata Rak Manuel Schiff Guido Kroemer Massimo Zeviani Pierre Rustin

Mice with the hypomorphic AIF-Harlequin mutation exhibit a highly heterogeneous mitochondriopathy that mostly affects respiratory chain complex I, causing a cerebral pathology that resembles that found in patients with AIF loss-of-function mutations. Here we describe that the antidiabetic drug pioglitazone (PIO) can improve the phenotype of a mouse Harlequin (Hq) subgroup, presumably due to an ...

Journal: :The Journal of Pediatric Research 2015

Journal: :British Journal of Anaesthesia 2007

Journal: :Journal of Diagnostic Medical Sonography 1999

2017
Belide Shruthi B.R. Nilgar Anita Dalal Nehaben Limbani

Harlequin ichthyosis is a very rare condition that affects the skin of newborns. It is associated with poor barrier function of the skin leading to dehydration and leaves newborns prone to infections. It is due to mutations in adenosine triphosphate binding cassette A12 gene transmitted as an autosomal recessive disorder. The prognosis is very poor in these cases. Here, we report one such rare ...

2013
Hyun Soo Lee Simona Schlereth Payal Khandelwal Daniel R. Saban

A reproducible method to inhibit allergic immune responses is accomplished with hi-dose Ag sensitization, via intraperitoneal (IP) injection. However, the role of CD4+ CD25+ FoxP3+ T regulatory cells (Treg) in this process is unknown, as is whether such modulation extends to ocular allergy. We therefore determined herein whether hi-dose sensitization modulates ocular allergy, and whether CD4+ C...

Journal: :Clinical journal of sport medicine : official journal of the Canadian Academy of Sport Medicine 2012
Andrew W Harris Donald C Voaklander C Allyson Jones Brian H Rowe

OBJECTIVE To provide population-based risk estimates for sustaining subsequent head injuries (HIs), which occur in sports and recreation (SR). DESIGN Population-based, retrospective, cross-sectional study. SETTING Retrospective review of data from 2 tertiary care and 3 community care emergency departments (EDs) in Edmonton, Alberta, Canada. PATIENTS Individuals younger than 36 years prese...

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