Peer-Zada AA - Search Results

1

Novel de novo heterozygous CACNA1A gene variant in generalised dystonia: a case report.

Alshareet M, Alakkas A, Alsinaidi OA, Bawazeer S, Peer-Zada AA. Alshareet M, et al. Among authors: peer zada aa. BMJ Neurol Open. 2024 Jun 21;6(1):e000710. doi: 10.1136/bmjno-2024-000710. eCollection 2024. BMJ Neurol Open. 2024. PMID: 38912174 Free PMC article.

2

A rare presentation of BCR-ABL1 and RUNX1-MECOM rearrangement in a pediatric patient with acute myeloid leukemia.

Alamri RM, Alanazi M, AlRajeh RK, Tashkandi SA, Alswayyed AF, Samman MA, Peer-Zada AA. Alamri RM, et al. Among authors: peer zada aa. Clin Case Rep. 2024 May 14;12(5):e8917. doi: 10.1002/ccr3.8917. eCollection 2024 May. Clin Case Rep. 2024. PMID: 38751957 Free PMC article.

3

Favorable outcome of PML-RARα short isoform and FLT3-ITD mutation in a patient with several adverse prognostic markers: A case report.

Bafail MA, AlTahan R, Samman MA, Tashkandi SA, Motabi IH, Peer-Zada AA. Bafail MA, et al. Among authors: peer zada aa. Clin Case Rep. 2023 Jul 6;11(7):e07637. doi: 10.1002/ccr3.7637. eCollection 2023 Jul. Clin Case Rep. 2023. PMID: 37426684 Free PMC article.

4

Excessive homozygosity identified by chromosomal microarray at a known GCDH mutation locus correlates with brain MRI abnormalities in an infant with glutaric aciduria.

Peer-Zada AA, Al-Asmari AM. Peer-Zada AA, et al. Clin Case Rep. 2017 Jun 28;5(8):1303-1308. doi: 10.1002/ccr3.1054. eCollection 2017 Aug. Clin Case Rep. 2017. PMID: 28781846 Free PMC article.

5

Atypical presentation of adenosine deaminase 2 deficiency with bi-allelic ADA2 mutation.

Al-Shaikh R, Alnowaiser D, Peer-Zada AA, Almutairi A, Alghamdi H. Al-Shaikh R, et al. Among authors: peer zada aa. Clin Case Rep. 2022 Mar 1;10(3):e05408. doi: 10.1002/ccr3.5408. eCollection 2022 Mar. Clin Case Rep. 2022. PMID: 35261770 Free PMC article.

6

Fatal intracranial haemorrhage in acute promyelocytic leukemia patients with short isoform of PML-RARα: Review of molecular and radiological data.

Abudawood M, Alorini H, Samman MA, Bashir SM, AlSwayed A, Binhassan S, Peer-Zada AA. Abudawood M, et al. Among authors: peer zada aa. Saudi J Biol Sci. 2023 Jul;30(7):103710. doi: 10.1016/j.sjbs.2023.103710. Epub 2023 Jun 19. Saudi J Biol Sci. 2023. PMID: 37405260 Free PMC article.

7

Use of Array Comparative Genomic Hybridization for the Diagnosis of DiGeorge Syndrome in Saudi Arabian Population.

Bahamat AA, Assidi M, Lary SA, Almughamsi MM, Peer Zada AA, Chaudhary A, Abuzenadah A, Abu-Elmagd M, Al-Qahtani M. Bahamat AA, et al. Among authors: peer zada aa. Cytogenet Genome Res. 2018;154(1):20-29. doi: 10.1159/000487094. Epub 2018 Feb 17. Cytogenet Genome Res. 2018. PMID: 29455205

8

Development of simple and effective PCR based assay to detect PCCA mutation (c.425G > A) among Saudi carriers and functional study of the homozygous PCCA mutations.

Al-Asmari A, Peer-Zada AA, AlDehaimi A, Polychronakos C, Chentoufi AA. Al-Asmari A, et al. Among authors: peer zada aa. Saudi J Biol Sci. 2022 Dec;29(12):103461. doi: 10.1016/j.sjbs.2022.103461. Epub 2022 Sep 27. Saudi J Biol Sci. 2022. PMID: 36211601 Free PMC article.

9

High expression of matrix metalloproteinases: MMP-2 and MMP-9 predicts poor survival outcome in colorectal carcinoma.

Salem N, Kamal I, Al-Maghrabi J, Abuzenadah A, Peer-Zada AA, Qari Y, Al-Ahwal M, Al-Qahtani M, Buhmeida A. Salem N, et al. Future Oncol. 2016 Feb;12(3):323-31. doi: 10.2217/fon.15.325. Epub 2016 Jan 19. Future Oncol. 2016. PMID: 26814712

10

New paradigms of USP53 disease: normal GGT cholestasis, BRIC, cholangiopathy, and responsiveness to rifampicin.

Alhebbi H, Peer-Zada AA, Al-Hussaini AA, Algubaisi S, Albassami A, AlMasri N, Alrusayni Y, Alruzug IM, Alharby E, Samman MA, Ayoub SZ, Maddirevula S, Peake RWA, Alkuraya FS, Wali S, Almontashiri NAM. Alhebbi H, et al. Among authors: peer zada aa. J Hum Genet. 2021 Feb;66(2):151-159. doi: 10.1038/s10038-020-0811-1. Epub 2020 Aug 6. J Hum Genet. 2021. PMID: 32759993

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