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Pattern of steroid resistant nephrotic syndrome in children living in the kingdom of Saudi Arabia: a single center study.
Saudi J Kidney Dis Transpl. 2009 Sep;20(5):854-7.
Saudi J Kidney Dis Transpl. 2009.
PMID: 19736491
Renal involvement in children with spina bifida.
Kari JA, Safdar O, Jamjoom R, Anshasi W.
Kari JA, et al. Among authors: anshasi w.
Saudi J Kidney Dis Transpl. 2009 Jan;20(1):102-5.
Saudi J Kidney Dis Transpl. 2009.
PMID: 19112226
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Histopathology of steroid-resistant nephrotic syndrome in children living in the Kingdom of Saudi Arabia.
Kari JA, Halawani M, Mokhtar G, Jalalah SM, Anshasi W.
Kari JA, et al. Among authors: anshasi w.
Pediatr Nephrol. 2009 Jul;24(7):1429-30. doi: 10.1007/s00467-008-1106-5. Epub 2009 Jan 17.
Pediatr Nephrol. 2009.
PMID: 19152008
No abstract available.
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A new focus of autochthonous transmission of Cordylobia anthropophaga in Saudi Arabia.
Afifi MA, Jiman-Fatani AA, Alsiny FI, Anshasi WS.
Afifi MA, et al. Among authors: anshasi ws.
J Microsc Ultrastruct. 2015 Apr-Jun;3(2):82-85. doi: 10.1016/j.jmau.2014.12.002. Epub 2015 Jan 19.
J Microsc Ultrastruct. 2015.
PMID: 30023186
Free PMC article.
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Exome analysis identified a novel missense mutation in the CLPP gene in a consanguineous Saudi family expanding the clinical spectrum of Perrault Syndrome type-3.
Ahmed S, Jelani M, Alrayes N, Mohamoud HS, Almramhi MM, Anshasi W, Ahmed NA, Wang J, Nasir J, Al-Aama JY.
Ahmed S, et al. Among authors: anshasi w.
J Neurol Sci. 2015;353(1-2):149-54. doi: 10.1016/j.jns.2015.04.038. Epub 2015 May 1.
J Neurol Sci. 2015.
PMID: 25956234
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Novel nonsense mutation in the PTRF gene underlies congenital generalized lipodystrophy in a consanguineous Saudi family.
Jelani M, Ahmed S, Almramhi MM, Mohamoud HS, Bakur K, Anshasi W, Wang J, Al-Aama JY.
Jelani M, et al. Among authors: anshasi w.
Eur J Med Genet. 2015 Apr;58(4):216-21. doi: 10.1016/j.ejmg.2015.02.002. Epub 2015 Feb 23.
Eur J Med Genet. 2015.
PMID: 25721873
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