Yavarian M - Search Results

1

PCDH19-clustering epilepsy, pathophysiology and clinical significance.

Kowkabi S, Yavarian M, Kaboodkhani R, Mohammadi M, Shervin Badv R. Kowkabi S, et al. Among authors: yavarian m. Epilepsy Behav. 2024 May;154:109730. doi: 10.1016/j.yebeh.2024.109730. Epub 2024 Mar 22. Epilepsy Behav. 2024. PMID: 38521028 Review.

2

Retraction Note: The toxicity and therapeutic effects of single-and multi-wall carbon nanotubes on mice breast cancer.

Kavosi A, Noei SHG, Madani S, Khalighfard S, Khodayari S, Khodayari H, Mirzaei M, Kalhori MR, Yavarian M, Alizadeh AM, Falahati M. Kavosi A, et al. Among authors: yavarian m. Sci Rep. 2023 Nov 15;13(1):19953. doi: 10.1038/s41598-023-46596-w. Sci Rep. 2023. PMID: 37968356 Free PMC article. No abstract available.

3

Generalized exfoliative skin rash as an early predictor of supratherapeutic voriconazole trough levels in a leukemic child: A case report.

Amanati A, Badiee P, Lotfi M, Monabati A, Faghihi MA, Yavarian M, Hatami Mazinani N. Amanati A, et al. Among authors: yavarian m. Curr Med Mycol. 2020 Sep;6(3):73-78. doi: 10.18502/cmm.6.3.4500. Curr Med Mycol. 2020. PMID: 33834148 Free PMC article.

4

Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder.

Polla DL, Farazi Fard MA, Tabatabaei Z, Habibzadeh P, Levchenko OA, Nikuei P, Makrythanasis P, Hussain M, von Hardenberg S, Zeinali S, Fallah MS, Schuurs-Hoeijmakers JHM, Shahzad M, Fatima F, Fatima N, Kaat LD, Bruggenwirth HT, Fleming LR, Condie J, Ploski R, Pollak A, Pilch J, Demina NA, Chukhrova AL, Sergeeva VS, Venselaar H, Masri AT, Hamamy H, Santoni FA, Linda K, Ahmed ZM, Nadif Kasri N, de Brouwer APM, Bergmann AK, Hethey S, Yavarian M, Ansar M, Riazuddin S, Riazuddin S, Silawi M, Ruggeri G, Pirozzi F, Eftekhar E, Taghipour Sheshdeh A, Bahramjahan S, Mirzaa GM, Lavrov AV, Antonarakis SE, Faghihi MA, van Bokhoven H. Polla DL, et al. Among authors: yavarian m. Genet Med. 2021 Jul;23(7):1246-1254. doi: 10.1038/s41436-021-01133-w. Epub 2021 Apr 6. Genet Med. 2021. PMID: 33824500 Free PMC article.

5

Role of the 820 A/G variant in the IGF-2 gene and recurrent spontaneous abortion in southern Iran: A cross-sectional study.

Ardeshir F, Keshavarz L, Asadian F, Omidmokhtarkhanloo G, Yavarian M. Ardeshir F, et al. Among authors: yavarian m. Int J Reprod Biomed. 2020 Sep 20;18(9):747-754. doi: 10.18502/ijrm.v13i9.7669. eCollection 2020 Sep. Int J Reprod Biomed. 2020. PMID: 33062920 Free PMC article.

6

Potential voriconazole associated posterior reversible leukoencephalopathy in children with malignancies: Report of two cases.

Amanati A, Lotfi M, Manen RV, Faghihi MA, Yavarian M, Zekavat O, Badiee P, Mazinani NH, Bozorgi H. Amanati A, et al. Among authors: yavarian m. J Oncol Pharm Pract. 2021 Mar;27(2):498-504. doi: 10.1177/1078155220941590. Epub 2020 Jul 20. J Oncol Pharm Pract. 2021. PMID: 32689868

7

A novel stop-gain mutation in DPYS gene causing Dihidropyrimidinase deficiency, a case report.

Mirzaei M, Kavosi A, Sharifzadeh M, Mahjoub G, Faghihi MA, Habibzadeh P, Yavarian M. Mirzaei M, et al. Among authors: yavarian m. BMC Med Genet. 2020 Jun 29;21(1):138. doi: 10.1186/s12881-020-01070-6. BMC Med Genet. 2020. PMID: 32600357 Free PMC article.

8

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. Among authors: yavarian m. BMC Gastroenterol. 2020 May 8;20(1):142. doi: 10.1186/s12876-020-01280-5. BMC Gastroenterol. 2020. PMID: 32384880 Free PMC article.

9

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. Among authors: yavarian m. Front Neurol. 2019 Sep 4;10:944. doi: 10.3389/fneur.2019.00944. eCollection 2019. Front Neurol. 2019. PMID: 31551910 Free PMC article.

10

The association of Q472H variant in the KDR gene with recurrent pregnancy loss in Southern Iran: A case-control study.

Keshavarz L, Yavarian M. Keshavarz L, et al. Among authors: yavarian m. Int J Reprod Biomed. 2019 Jul 31;17(7):473-480. doi: 10.18502/ijrm.v17i7.4858. eCollection 2019 Jul. Int J Reprod Biomed. 2019. PMID: 31508572 Free PMC article.

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