Housawi Y - Search Results

1

SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population.

Mir A, Almudhry M, Alghamdi F, Albaradie R, Ibrahim M, Aldurayhim F, Alhedaithy A, Alamr M, Bawazir M, Mohammad S, Abdelhay S, Bashir S, Housawi Y. Mir A, et al. Among authors: housawi y. Hum Genet. 2022 Jan;141(1):81-99. doi: 10.1007/s00439-021-02404-x. Epub 2021 Nov 19. Hum Genet. 2022. PMID: 34797406

2

Epilepsy in patients with EAST syndrome caused by mutation in the KCNJ10.

Mir A, Chaudhary M, Alkhaldi H, Alhazmi R, Albaradie R, Housawi Y. Mir A, et al. Among authors: housawi y. Brain Dev. 2019 Sep;41(8):706-715. doi: 10.1016/j.braindev.2019.03.009. Epub 2019 Apr 2. Brain Dev. 2019. PMID: 30952461 Review.

3

Corrigendum to "Epilepsy in patients with EAST syndrome caused by mutation in the KCNJ10" [Brain Dev 2019].

Mir A, Chaudhary M, Alkhaldi H, Alhazmi R, Albaradie R, Housawi Y. Mir A, et al. Among authors: housawi y. Brain Dev. 2019 Sep;41(8):716. doi: 10.1016/j.braindev.2019.06.007. Epub 2019 Jul 19. Brain Dev. 2019. PMID: 31331637 No abstract available.

4

Complete resolution of epileptic spasms with vigabatrin in a patient with 3-methylglutaconic aciduria caused by TIMM50 gene mutation.

Mir A, Hadab S, Sammak M, Alhazmi R, Housawi Y, Bashir S. Mir A, et al. Among authors: housawi y. Clin Genet. 2020 Jul;98(1):102-103. doi: 10.1111/cge.13763. Epub 2020 May 5. Clin Genet. 2020. PMID: 32369862 No abstract available.

5

Continuous Spikes and Waves During Sleep (CSWS), Severe Epileptic Encephalopathy, and Choreoathetosis due to Mutations in FRRS1L.

Mir A, Amer F, Ali M, Alotaibi W, Alotaibi M, Hedaithy A, Aldurayhim F, Hussain F, Bashir S, Housawi Y. Mir A, et al. Among authors: housawi y. Clin EEG Neurosci. 2023 Sep;54(5):526-533. doi: 10.1177/15500594221112508. Epub 2022 Jul 11. Clin EEG Neurosci. 2023. PMID: 35815844

6

Constitutional Mismatch Repair Deficiency Syndromes, a Neurofibromatosis 1 Mimicker That Hinders Timely Management.

Mir A, AlMudhry M, AlOtaibi W, AlHazmi R, AlBaradie R, AlHarbi Q, Bashir S, Chamdine O, Housawi Y. Mir A, et al. Among authors: housawi y. J Pediatr Hematol Oncol. 2023 Jul 1;45(5):e613-e620. doi: 10.1097/MPH.0000000000002641. Epub 2023 Feb 20. J Pediatr Hematol Oncol. 2023. PMID: 36897649

7

Loss-of-Function Mutations in KIF15 Underlying a Braddock-Carey Genocopy.

Sleiman PMA, March M, Nguyen K, Tian L, Pellegrino R, Hou C, Dridi W, Sager M, Housawi YH, Hakonarson H. Sleiman PMA, et al. Among authors: housawi yh. Hum Mutat. 2017 May;38(5):507-510. doi: 10.1002/humu.23188. Epub 2017 Mar 10. Hum Mutat. 2017. PMID: 28150392

8

Screening for Lynch syndrome in young Saudi colorectal cancer patients using microsatellite instability testing and next generation sequencing.

Alqahtani M, Edwards C, Buzzacott N, Carpenter K, Alsaleh K, Alsheikh A, Abozeed W, Mashhour M, Almousa A, Housawi Y, Al Hawwaj S, Iacopetta B. Alqahtani M, et al. Among authors: housawi y. Fam Cancer. 2018 Apr;17(2):197-203. doi: 10.1007/s10689-017-0015-9. Fam Cancer. 2018. PMID: 28643016

9

Benign familial and non-familial infantile seizures (Fukuyama-Watanabe-Vigevano syndrome): a study of 14 cases from Saudi Arabia.

Saadeldin IY, Housawi Y, Al Nemri A, Al Hifzi I. Saadeldin IY, et al. Among authors: housawi y. Brain Dev. 2010 May;32(5):378-84. doi: 10.1016/j.braindev.2009.04.014. Epub 2009 May 22. Brain Dev. 2010. PMID: 19464832

10

A missense mutation in ANKRD26 segregates with thrombocytopenia.

Al Daama SA, Housawi YH, Dridi W, Sager M, Otieno FG, Hou C, Vasquez L, Kim C, Tian L, Sleiman P, Hakonarson H. Al Daama SA, et al. Blood. 2013 Jul 18;122(3):461-2. doi: 10.1182/blood-2013-03-489344. Blood. 2013. PMID: 23869080 Free article. No abstract available.

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