Ahmed AA - Search Results

1

Ewing sarcoma family of tumors in unusual sites: confirmation by rt-PCR.

Ahmed AA, Nava VE, Pham T, Taubenberger JK, Lichy JH, Sorbara L, Raffeld M, Mackall CL, Tsokos M. Ahmed AA, et al. Pediatr Dev Pathol. 2006 Nov-Dec;9(6):488-95. doi: 10.2350/06-01-0007.1. Pediatr Dev Pathol. 2006. PMID: 17163788

2

Sinonasal rhabdomyosarcoma in children and young adults.

Ahmed AA, Tsokos M. Ahmed AA, et al. Int J Surg Pathol. 2007 Apr;15(2):160-5. doi: 10.1177/1066896906299122. Int J Surg Pathol. 2007. PMID: 17478770

3

Expression of c-kit in Ewing family of tumors: a comparison of different immunohistochemical protocols.

Ahmed A, Gilbert-Barness E, Lacson A. Ahmed A, et al. Pediatr Dev Pathol. 2004 Jul-Aug;7(4):342-7. doi: 10.1007/s10024-002-0077-y. Epub 2004 Jun 17. Pediatr Dev Pathol. 2004. PMID: 15383930

4

Immunohistochemical expression of endothelial nitric oxide synthase and C-kit in the placenta of complete hydatidiform mole.

Ahmed A, Lacson A, Gilbert-Barness E. Ahmed A, et al. Fetal Pediatr Pathol. 2005 May-Jun;24(3):141-7. doi: 10.1080/15227950500304200. Fetal Pediatr Pathol. 2005. PMID: 16338875

5

Pathology teach and tell: fibrinogen storage disease in a child with hypofibrinogenemia and decreased ceruloplasmin.

Bruzzi C, Bader A, Luban NL, Przygodzki R, Ahmed AA. Bruzzi C, et al. Among authors: ahmed aa. Fetal Pediatr Pathol. 2007 Mar-Apr;26(2):101-5. doi: 10.1080/15513810701448623. Fetal Pediatr Pathol. 2007. PMID: 17701692

6

Complex congenital heart defects in association with maternal diabetes and partial deletion of the A2BP1 gene.

Lale S, Yu S, Ahmed A. Lale S, et al. Fetal Pediatr Pathol. 2011;30(3):161-6. doi: 10.3109/15513815.2010.547555. Epub 2011 Feb 28. Fetal Pediatr Pathol. 2011. PMID: 21355681

7

Adrenocortical neoplasms in young children: age as a prognostic factor.

Ahmed AA. Ahmed AA. Ann Clin Lab Sci. 2009 Summer;39(3):277-82. Ann Clin Lab Sci. 2009. PMID: 19667412

8

Placenta membranacea: a developmental anomaly with diverse clinical presentation.

Ahmed A, Gilbert-Barness E. Ahmed A, et al. Pediatr Dev Pathol. 2003 Mar-Apr;6(2):201-2. doi: 10.1007/s10024-002-0007-z. Epub 2003 Jan 21. Pediatr Dev Pathol. 2003. PMID: 12532260 No abstract available.

9

A Fryns syndrome-like phenotype with mosaic t(1;22)(q12;p12) chromosomal translocation.

Ahmed AA, Gilbert-Barness E. Ahmed AA, et al. Clin Dysmorphol. 2004 Apr;13(2):111-112. Clin Dysmorphol. 2004. PMID: 15057129

10

Congenital disorder of glycosylation-X: clinicopathologic study of an autopsy case with distinct neuropathologic features.

Agarwal B, Ahmed A, Rushing EJ, Bloom M, Kadom N, Vezina G, Krasnewich D, Santi M. Agarwal B, et al. Hum Pathol. 2007 Nov;38(11):1714-9. doi: 10.1016/j.humpath.2007.05.028. Hum Pathol. 2007. PMID: 17954208

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