الفهرسة نشطة
للباحثين للناشرين تسجيل الدخول إنشاء حساب
الرئيسية المؤلفون Heba Salah
HS

Heba Salah

h-4 H-Index
46 Citations
17 Papers

Published Papers

17 indexed
1
Selective screening in neonates suspected to have inborn errors of metabolism
Egyptian Journal of Medical Human Genetics Q2 2015 10.1016/j.ejmhg.2015.01.003
13 citations 386
2
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
3
Demographic and clinical features of glutaric acidemia type 1; a high frequency among isolates in Upper Egypt
Egyptian Journal of Medical Human Genetics Q2 2014 10.1016/j.ejmhg.2014.01.001
5 citations 391
4
Molecular characterization of X chromosome fragility in idiopathic mental retardation
Egyptian Journal of Medical Human Genetics Q2 2016 10.1016/j.ejmhg.2015.11.001
4 citations 391
5
Intrafamilial variability in Simpson–Golabi–Behmel syndrome with bilateral posterior ear lobule creases
Egyptian Journal of Medical Human Genetics Q2 2014 10.1016/j.ejmhg.2013.08.001
3 citations 391
6
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
7
Bilateral iris, choroid, optic nerve colobomas and retinal detachment in an Egyptian patient with mild Baraitser–Winter syndrome
Egyptian Journal of Medical Human Genetics Q2 2014 10.1016/j.ejmhg.2013.11.001
2 citations 391
8
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 393
9
Chromosomal abnormalities and autism
Egyptian Journal of Medical Human Genetics Q2 2016 10.1016/j.ejmhg.2015.05.002
2 citations 386
10
Cardiological assessment of a cohort of Egyptian patients with osteogenesis imperfecta type III
Egyptian Journal of Medical Human Genetics Q2 2016 10.1016/j.ejmhg.2015.12.004
2 citations 383
11
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
12
Bilateral absence of fifth ray in feet, cleft palate, malformed ears, and corneal opacity in a patient with Miller syndrome
Egyptian Journal of Medical Human Genetics Q2 2014 10.1016/j.ejmhg.2013.12.004
1 citations 393
13
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
14
Effect of Mannitol on Renal Function during Cardiac Surgery and Immediate Post-Operative in Selected Private Hospitals in Nablus City/ Palestine
Jordan Journal of Pharmaceutical Sciences Q2 2025 10.35516/jjps.v18i2.2640
1 citations 387
15
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
16
The existence of an international dispute is a condition for accepting a lawsuit before the International Court of Justice
Journal of Anbar University for Law and Political Sciences Q4 2024 10.37651/aujlps.2024.153769.1359
0 citations 384
17
Prevalence of congenital heart defects among 54 Egyptian children with Maple syrup urine disease
Egyptian Journal of Medical Human Genetics Q2 2018 10.1016/j.ejmhg.2017.10.001
0 citations 389

Publication Activity

Journals Published In

Egyptian Journal of Medical Human Genetics
🇪🇬 Q2 AMS 99
Egyptian Journal of Medical Human Genetics
🇪🇬 Q2 AMS 98
Jordan Journal of Pharmaceutical Sciences
🇯🇴 Q2 AMS 87
Journal of Anbar University for Law and Political Sciences
🇮🇶 Q4 AMS 42