نتایج جستجو برای: sulzberger disease

تعداد نتایج: 1490508  

2008
A Van Wijk Ed

Status of This Memo This memo provides information for the Internet community. It does not specify an Internet standard of any kind. Distribution of this memo is unlimited. Abstract This document lists the essential requirements for real-time Text-over-IP (ToIP) and defines a framework for implementation of all required functions based on the Session Initiation Protocol (SIP) and the Real-Time ...

Journal: :Physical review. E, Statistical, nonlinear, and soft matter physics 2001
D Michaelis U Peschel F Lederer D V Skryabin W J Firth

We identify a universal criterion for the onset of a nonequilibrium Ising-Bloch (NIB) transition, and describe the behavior near the bifurcation by a generic amplitude equation. We found that a NIB transition is caused by an antisymmetric eigenvector passing the translational mode of the system at a critical point. In this context we discuss Hamiltonian and dissipative systems. We report on a N...

2017
PRAVEEN KUMAR RATHORE

Incontinentia pigmenti (IP) is a X-linked dominant neuro cutaneous syndrome with cutaneous, neurologic, ophthalmologic and dental manifestations mainly in female neonates. Starting from neonatal period, IP passes through stages of vesicular (90%), verrucous (70%), hyper pigmented (98%) and hypopigmented lesions. Authors report a case of IP in 8 months old female child who presented with vesicul...

2011
Gabriele Basilico Vieri del Bianco Luigi Lavazza Sandro Morasca Davide Taibi Davide Tosi

for dissemination)

Journal: :American journal of ophthalmology 1966
D Miller

Sulzberger syndrome (incbntinentia pigmenti.) pigmenti associated with changes in the posterior Brit. J. Ophth. 39:276, 1955. chamber of the eye. Am. J. Ophth. 47 :321, 1959. 7. Kriimmel, H., and Rausch, L.: Anomalien 9. Reese, A. B.: Persistent hyperplastic primades Auges bei der sogenannten Incontinentia pigry vitreous. Am. J. Ophth. 40:317, 1955. menti. Ophthalmologica, 130:31, 1955. 10. Jon...

انصاری, قاسم, فریدونی, محمودرضا,

سابقه و هدف: (IP) Incontinentia pigmenti یا سندرم Bloch-Sulzberger اولین بار توسط Garrod در سال 1906 معرفی گردید. سپس، در سال 1926 توسط Bloch و در سال 1927 توسط Sulzberger گزارش شد. این بیماری یک بیماری ژنتیکی پوستی است که از نظر توارث وابسته به جنس غالب می باشد. ماکول های نامنظم، شیر قهوه ای یا خاکستری یا ضایعات آتروفیک، فرورفته و دپیگمانته از علایم پوستی این بیماری می باشند. هدف مقاله حاضر مع...

Journal: :Journal of interprofessional care 2012
Esther Suter Siegrid Deutschlander Grace Mickelson Zahra Nurani Jana Lait Liz Harrison Sandra Jarvis-Selinger Lesley Bainbridge Sheila Achilles Christine Ateah Kendall Ho Ruby Grymonpre

Many studies examine the impact of interprofessional (IP) interventions on various health practice and education outcomes. One significant gap is the lack of research on the effects of IP interventions on health human resource (HHR) outcomes. This project synthesized the literature on the impact of IP interventions at the pre- and post-licensure levels on quality workplace, staff satisfaction, ...

Journal: :JAMA neurology 2015
Deepali Eksambe Nnenna Agim Naseem Uddin Garrett Gotway Juan M Pascual

IKBKGMutationWith Incontinentia Pigmenti and Ring-Enhancing Encephalopathy Incontinentia pigmenti (IP, Bloch-Sulzberger syndrome) is an X-linkeddominantgenodermatosis affectingskinandotherorgans, including the brain, with variable expressivity. Incontinentia pigmenti results frommutations in the inhibitor of κ-βkinase-γ gene (IKBKG),which is locatedonXq28.Deletions in this gene result in loss o...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید