Habibzadeh P - Search Results

1

Molecular diagnostic assays for COVID-19: an overview.

Habibzadeh P, Mofatteh M, Silawi M, Ghavami S, Faghihi MA. Habibzadeh P, et al. Crit Rev Clin Lab Sci. 2021 Sep;58(6):385-398. doi: 10.1080/10408363.2021.1884640. Epub 2021 Feb 17. Crit Rev Clin Lab Sci. 2021. PMID: 33595397 Free PMC article. Review.

2

The potential effectiveness of acetazolamide in the prevention of acute kidney injury in COVID-19: A hypothesis.

Habibzadeh P, Mofatteh M, Ghavami S, Roozbeh J. Habibzadeh P, et al. Eur J Pharmacol. 2020 Dec 5;888:173487. doi: 10.1016/j.ejphar.2020.173487. Epub 2020 Aug 15. Eur J Pharmacol. 2020. PMID: 32805256 Free PMC article.

3

Clinical and molecular characterization of a patient with mitochondrial Neurogastrointestinal Encephalomyopathy.

Habibzadeh P, Silawi M, Dastsooz H, Bahramjahan S, Ezzatzadegan Jahromi S, Ostovan VR, Yavarian M, Mofatteh M, Faghihi MA. Habibzadeh P, et al. BMC Gastroenterol. 2020 May 8;20(1):142. doi: 10.1186/s12876-020-01280-5. BMC Gastroenterol. 2020. PMID: 32384880 Free PMC article.

4

A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case report.

Ziyaee F, Shorafa E, Dastsooz H, Habibzadeh P, Nemati H, Saeed A, Silawi M, Farazi Fard MA, Faghihi MA, Dastgheib SA. Ziyaee F, et al. Among authors: habibzadeh p. BMC Med Genet. 2019 Jan 14;20(1):13. doi: 10.1186/s12881-018-0743-1. BMC Med Genet. 2019. PMID: 30642275 Free PMC article.

5

A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment.

Habibzadeh P, Inaloo S, Silawi M, Dastsooz H, Farazi Fard MA, Sadeghipour F, Faghihi Z, Rezaeian M, Yavarian M, Böhm J, Faghihi MA. Habibzadeh P, et al. Front Neurol. 2019 Sep 4;10:944. doi: 10.3389/fneur.2019.00944. eCollection 2019. Front Neurol. 2019. PMID: 31551910 Free PMC article.

6

Expanding the molecular and clinical phenotypes of FUT8-CDG.

Ng BG, Dastsooz H, Silawi M, Habibzadeh P, Jahan SB, Fard MAF, Halliday BJ, Raymond K, Ruzhnikov MRZ, Tabatabaei Z, Taghipour-Sheshdeh A, Brimble E, Robertson SP, Faghihi MA, Freeze HH. Ng BG, et al. Among authors: habibzadeh p. J Inherit Metab Dis. 2020 Jul;43(4):871-879. doi: 10.1002/jimd.12221. Epub 2020 Feb 23. J Inherit Metab Dis. 2020. PMID: 32049367 Free PMC article.

7

Pre-Implantation Genetic Testing for Monogenic Disorders (PGT-M) in A Family with A Novel Mutation in DPAGT1 Gene.

Tabatabaei Z, Karbalaie KH, Habibzadeh P, Farazi Fard MA, Faghihi MA, Nasr Esfahani MH. Tabatabaei Z, et al. Among authors: habibzadeh p. Cell J. 2021 Oct;23(5):593-597. doi: 10.22074/cellj.2021.7335. Epub 2021 Oct 30. Cell J. 2021. PMID: 34837688 Free PMC article.

8

HDAC Inhibitors Induce BDNF Expression and Promote Neurite Outgrowth in Human Neural Progenitor Cells-Derived Neurons.

Bagheri A, Habibzadeh P, Razavipour SF, Volmar CH, Chee NT, Brothers SP, Wahlestedt C, Mowla SJ, Faghihi MA. Bagheri A, et al. Among authors: habibzadeh p. Int J Mol Sci. 2019 Mar 5;20(5):1109. doi: 10.3390/ijms20051109. Int J Mol Sci. 2019. PMID: 30841499 Free PMC article.

9

Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: a case series.

Mahjoub G, Habibzadeh P, Dastsooz H, Mirzaei M, Kavosi A, Jamali L, Javanmardi H, Katibeh P, Faghihi MA, Dastgheib SA. Mahjoub G, et al. Among authors: habibzadeh p. BMC Med Genet. 2019 Oct 29;20(1):167. doi: 10.1186/s12881-019-0893-9. BMC Med Genet. 2019. PMID: 31664948 Free PMC article.

10

Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.

Habibzadeh P, Tabatabaei Z, Inaloo S, Nashatizadeh MM, Synofzik M, Ostovan VR, Faghihi MA. Habibzadeh P, et al. Front Genet. 2020 Dec 22;11:585136. doi: 10.3389/fgene.2020.585136. eCollection 2020. Front Genet. 2020. PMID: 33414805 Free PMC article.

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