Hassan HH - Search Results

1

JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency.

Alsohime F, Martin-Fernandez M, Temsah MH, Alabdulhafid M, Le Voyer T, Alghamdi M, Qiu X, Alotaibi N, Alkahtani A, Buta S, Jouanguy E, Al-Eyadhy A, Gruber C, Hasan GM, Bashiri FA, Halwani R, Hassan HH, Al-Muhsen S, Alkhamis N, Alsum Z, Casanova JL, Bustamante J, Bogunovic D, Alangari AA. Alsohime F, et al. Among authors: hassan hh. N Engl J Med. 2020 Jan 16;382(3):256-265. doi: 10.1056/NEJMoa1905633. N Engl J Med. 2020. PMID: 31940699 Free PMC article.

2

ARL6IP6, a susceptibility locus for ischemic stroke, is mutated in a patient with syndromic Cutis Marmorata Telangiectatica Congenita.

Abumansour IS, Hijazi H, Alazmi A, Alzahrani F, Bashiri FA, Hassan H, Alhaddab M, Alkuraya FS. Abumansour IS, et al. Hum Genet. 2015 Aug;134(8):815-22. doi: 10.1007/s00439-015-1561-6. Epub 2015 May 10. Hum Genet. 2015. PMID: 25957586

3

Idiopathic intracranial hypertension in children: Diagnostic and management approach.

Albakr A, Hamad MH, Alwadei AH, Bashiri FA, Hassan HH, Idris H, Hassan S, Muayqil T, Altweijri I, Salih MA. Albakr A, et al. Among authors: hassan hh, hassan s. Sudan J Paediatr. 2016;16(2):67-76. Sudan J Paediatr. 2016. PMID: 28096561 Free PMC article.

4

Pediatric intracranial hypertension. Experience from 2 Tertiary Centers.

Bashiri FA, Al Abdulsalam HK, Hassan SM, Al Twaijri WA, Almalki FI, Kentab AY, Hamad MH, Alwadei AH, Al-Showaeir DA, Altweijri IS, Aldabjan HM, Aldegether MS, Albakr AA, Alhothali WM, Ajlan AM, Hassan HH, Salih MA. Bashiri FA, et al. Among authors: hassan sm, hassan hh. Neurosciences (Riyadh). 2019 Oct;24(4):257-263. doi: 10.17712/nsj.2019.4.20190052. Neurosciences (Riyadh). 2019. PMID: 31872803 Free PMC article.

5

A newly recognized autosomal recessive syndrome affecting neurologic function and vision.

Salih MA, Tzschach A, Oystreck DT, Hassan HH, AlDrees A, Elmalik SA, El Khashab HY, Wienker TF, Abu-Amero KK, Bosley TM. Salih MA, et al. Among authors: hassan hh. Am J Med Genet A. 2013 Jun;161A(6):1207-13. doi: 10.1002/ajmg.a.35850. Epub 2013 Apr 30. Am J Med Genet A. 2013. PMID: 23633300

6

Stroke due to mitochondrial disorders in Saudi children.

Salih MA, Abdel-Gader AG, Zahraa JN, Al-Rayess MM, Alorainy IA, Hassan HH, Ruitenbeek W, Zeviani M. Salih MA, et al. Among authors: hassan hh. Saudi Med J. 2006 Mar;27 Suppl 1:S81-90. Saudi Med J. 2006. PMID: 16532135

7

Perinatal stroke in Saudi children. Clinical features and risk factors.

Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Alorainy IA, Hassan HH, Al-Nasser MN. Salih MA, et al. Among authors: hassan hh. Saudi Med J. 2006 Mar;27 Suppl 1:S35-40. Saudi Med J. 2006. PMID: 16532129

8

Glutaric aciduria type 1 as a cause of dystonic cerebral palsy.

Mohamed S, Hamad MH, Hassan HH, Salih MA. Mohamed S, et al. Among authors: hassan hh. Saudi Med J. 2015 Nov;36(11):1354-7. doi: 10.15537/smj.2015.11.12132. Saudi Med J. 2015. PMID: 26593172 Free PMC article.

9

Stroke in Saudi children. Epidemiology, clinical features and risk factors.

Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Alorainy IA, Hassan HH, Bahakim HM, Kurbaan KM, Zahraa JN, Al-Nasser MN, Nasir AA, Khoja WA, Kabiraj MM. Salih MA, et al. Among authors: hassan hh. Saudi Med J. 2006 Mar;27 Suppl 1:S12-20. Saudi Med J. 2006. PMID: 16532126

10

Hematologic risk factors for stroke in Saudi children.

Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Alorainy IA, Hassan HH, Bahakim HM, Kurbaan KM, Zahraa JN, Murshid WR, El-Hazmi MA, Khoja WA. Salih MA, et al. Among authors: hassan hh. Saudi Med J. 2006 Mar;27 Suppl 1:S21-34. Saudi Med J. 2006. PMID: 16532128

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