الفهرسة نشطة
للباحثين للناشرين تسجيل الدخول إنشاء حساب
الرئيسية المؤلفون Shaimaa Abdelsattar Mohammad
SA

Shaimaa Abdelsattar Mohammad

h-3 H-Index
21 Citations
11 Papers

Published Papers

11 indexed
1
Meier-Gorlin syndrome: Report of an additional patient with congenital heart disease
Egyptian Journal of Medical Human Genetics Q2 2014 10.1016/j.ejmhg.2014.04.003
6 citations 393
2
Quantitative MR neurography of brachial plexus lesions based on diffusivity measurements
The Egyptian Journal of Radiology and Nuclear Medicine Q3 2018 10.1016/j.ejrnm.2018.05.005
5 citations 381
3
Unilateral proximal focal femoral deficiency, fibular aplasia, tibial campomelia and oligosyndactyly in an Egyptian child – Probable FFU syndrome
Egyptian Journal of Medical Human Genetics Q2 2014 10.1016/j.ejmhg.2014.03.001
3 citations 388
4
Oral-facial-digital syndrome with mesoaxial polysyndactyly, common AV canal, hirschsprung disease and sacral dysgenesis: Probably a transitional type between II, VI, variant of type VI or a new type
Egyptian Journal of Medical Human Genetics Q2 2014 10.1016/j.ejmhg.2014.02.004
2 citations 392
5
Cornelia-de Lange syndrome in an Egyptian infant with unusual bone deformities
Egyptian Journal of Medical Human Genetics Q2 2013 10.1016/j.ejmhg.2012.04.004
1 citations 388
6
Trichorhinophalangeal syndrome II, expanding the clinical spectrum
Egyptian Journal of Medical Human Genetics Q2 2015 10.1016/j.ejmhg.2014.05.007
1 citations 387
7
Baraitser–Winter syndrome: An additional Egyptian patient with skeletal anomalies, bilateral iris and choroid colobomas, retinal hypoplasia and hypoplastic scrotum
Egyptian Journal of Medical Human Genetics Q2 2016 10.1016/j.ejmhg.2015.04.004
1 citations 389
8
WITHDRAWN: Majewski Osteodysplastic Primordial Dwarfism, Type II with marked loss of subcutaneous fat, severe anemia, clenched hands and skeletal anomalies in an Egyptian patient
Egyptian Journal of Medical Human Genetics Q2 2017 10.1016/j.ejmhg.2017.08.008
1 citations 390
9
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II
Egyptian Journal of Medical Human Genetics Q2 2017 10.1016/j.ejmhg.2017.04.002
1 citations 387
10
Oral–Facial–Digital Syndrome type VI with self mutilations
Egyptian Journal of Medical Human Genetics Q2 2014 10.1016/j.ejmhg.2014.05.006
0 citations 391
11
Moebius syndrome with macular hyperpigmentation, skeletal anomalies, and hypoplasia of pectoralis major muscle in an Egyptian child
Egyptian Journal of Medical Human Genetics Q2 2015 10.1016/j.ejmhg.2014.10.003
0 citations 381

Publication Activity

Journals Published In

Egyptian Journal of Medical Human Genetics
🇪🇬 Q2 AMS 99
Egyptian Journal of Medical Human Genetics
🇪🇬 Q2 AMS 98
The Egyptian Journal of Radiology and Nuclear Medicine
🇪🇬 Q3 AMS 92