Infantile nephrotic syndrome with prominent facial dysmorphism: A possible case of Galloway-Mowat syndrome

Autor: Ahmed,Ayaz, Khalid,Adeel, Qaiser,Habib, Sajjad,Reema, Qader,Saima, Hashmi,Seema, Lanewala,Ali, Kazi,Javed Iqbal, Mubarak,Muhammed

Publikováno v: Portuguese Journal of Nephrology & Hypertension, Volume: 28, Issue: 2, Pages: 154-159, Published: JUN 2014
Portuguese Journal of Nephrology & Hypertension v.28 n.2 2014
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

Galloway-Mowat syndrome is a rare hereditary disorder originally described as a triad of early-onset nephrotic syndrome, microcephaly, and hiatus hernia. Subsequent reports have expanded the clinical and pathological spectrum of the disorder. We desc

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A Clinicopathologic Study of Primary Focal Segmental Glomerulosclerosis in Children.

Autor: Lanewala, Ali, Mubarak, Muhammed, Kazi, Javed Iqbal, Akhter, Fazal, Sher, Atika, Fayyaz, Amir, Bhatti, Sajid

Publikováno v: Saudi Journal of Kidney Diseases & Transplantation; May/Jun2012, Vol. 23 Issue 3, p513-520, 8p

Cellular and humoral immune responses in Campylobacter pylori-associated chronic gastritis.

Autor: Kazi, Javed Iqbal, Sinniah, Raja, Jaffrey, N. A., Alam, S. M., Zaman, V., Zuberi, S. J., Kazi, A. M.

Publikováno v: Journal of Pathology; 1989, Vol. 159 Issue 3, p231-237, 7p