نتایج جستجو برای: sulzberger disease

تعداد نتایج: 1490508  

2016
B. Thewes E. Davis A. Girgis P. C. Valery K. Giam A. Hocking J. Jackson V. Yf He D. Yip G. Garvey

BACKGROUND Indigenous Australians have poorer cancer outcomes in terms of incidence mortality and survival compared with non-Indigenous Australians. The factors contributing to this disparity are complex. Identifying and addressing the psychosocial factors and support needs of Indigenous cancer patients may help reduce this disparity. The Supportive Care Needs Assessment Tool for Indigenous Peo...

2015
Katja Hrovat Arnež Michaela Kindlova Nilesh J. Bokil James M. Murphy Matthew J. Sweet Gregor Gunčar

© 2015 The Author(s) Archiving permitted only in line with the archiving policy of Portland Press Limited. The final version of record will be available under the Creative Commons Attribution Licence 3.0 (http://creativecommons.org/licenses/by/3.0/). You are encouraged to use the final version of record. A C C E P T E D M A N U S C R IP T 10.1042/BSR20150246 . Please cite using the DOI 10.1042/...

2007
C. Perkins

This document adapts the Mobile IPv6 Fast Handovers to improve delay and packet loss resulting from Mobile IPv4 handover operations. Specifically, this document addresses movement detection, IP address configuration, and location update latencies during a handover. For reducing the IP address configuration latency, the document proposes that the new Care-of Address is always made to be the new ...

Journal: :Acta dermato-venereologica 2005
Mario Bittar Retno Danarti Arne König Andreas Gal Rudolf Happle

Sir, Incontinentia pigmenti (IP) is an X-linked dominant trait that is intrauterine lethal for males. The disorder is caused by NEMO mutations involving the NFkB activation pathway (1). It is characterized by linear skin lesions and various defects of the central nervous system, the teeth and the eyes. The cutaneous lesions are arranged along the lines of Blaschko, reflecting functional X-chrom...

Journal: :Journal of medical genetics 1995
T T Kirchman M L Levy R A Lewis M H Kanzler D L Nelson A E Scheuerle

Incontinentia pigmenti (IP) is a genodermatosis that segregates as an X linked dominant trait with male lethality. The disease has been linked to Xq28 in a number of studies. A few affected males have been documented, most of whom have a 47,XXY karyotype. We report a family with two paternally related half sisters, each affected with IP. The father is healthy, clinically normal, and has a 46,XY...

Journal: :Archivos de la Sociedad Espanola de Oftalmologia 2009
J Escudero F Borras M A Fernández C Domínguez

CASE REPORT The ophthalmic examination and results of fluorescein angiography using Retcam II are described in a patient with Incontinentia Pigmenti (IP). DISCUSSION Angiography fluorescein is extremely valuable in detecting vascular lesions that were invisible with ordinary ophthalmoscopy. Retcam II allows documentation of these lesions which is very useful for diagnosis, treatment and follo...

2014
D. PATEL G. V. RAVINDRA

Let X be a smooth projective variety over an algebraically closed field k of characteristic zero and Y ⊂ X a smooth ample hyperplane section. The Weak Lefschetz conjecture for Chow groups states that the natural restriction map CH(X)Q → CH(Y )Q is an isomorphism for all p < dim(Y )/2. In this note, we revisit a strategy introduced by Grothendieck to attack this problem by using the Bloch-Quille...

2013
D. PATEL G. V. RAVINDRA

Let X be a smooth projective variety over an algebraically closed field k ⊂ C of characteristic zero, and Y ⊂ X a smooth complete intersection. The Weak Lefschetz theorem states that the natural restriction map H(X(C), Q) → H(Y (C), Q) on singular cohomology is an isomorphism for all i < dim(Y ). The Bloch-Beilinson conjectures on the existence of certain filtrations on Chow groups combined wit...

Journal: :Journal of medical genetics 1982
T W Kurczynski J S Berns W E Johnson

A family is described in which incontinentia pigmenti (IP) is variably expressed in both sexes, compatible with either autosomal dominant or X linked dominant inheritance. This is the first reported instance of an affected male with a positive family history. Immunological studies of the proband showed no significant alteration of immune function. Cytogenetic investigations of the proband and h...

2014
M Tampa C Cirstoveanu Isabela Sarbu F Morar Clara Matei C Oancea V Benea Simona-Roxana Georgescu

Incontinentia pigmenti (IP) is a complex genodermatosis inherited in an X-linked dominant pattern, associating multistadial cutaneous manifestations with an oculo-dento-cerebral syndrome, which affects only female newborns, as the disorder is lethal in males since intrauterine period. We report on a case of incontinentia pigmenti with an atypical debut consisting of tonic-clonic seizures which ...

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