Farah R - Search Results

1

Lentiviral gene therapy corrects platelet phenotype and function in patients with Wiskott-Aldrich syndrome.

Sereni L, Castiello MC, Di Silvestre D, Della Valle P, Brombin C, Ferrua F, Cicalese MP, Pozzi L, Migliavacca M, Bernardo ME, Pignata C, Farah R, Notarangelo LD, Marcus N, Cattaneo L, Spinelli M, Giannelli S, Bosticardo M, van Rossem K, D'Angelo A, Aiuti A, Mauri P, Villa A. Sereni L, et al. Among authors: farah r. J Allergy Clin Immunol. 2019 Sep;144(3):825-838. doi: 10.1016/j.jaci.2019.03.012. Epub 2019 Mar 27. J Allergy Clin Immunol. 2019. PMID: 30926529 Free PMC article.

2

A Multicenter Experience from Lebanon in Childhood and Adolescent Acute Myeloid Leukemia: High rate of Early Death in Childhood Acute Promyelocytic Leukemia.

Farah RA, Horkos JG, Bustros YD, Farhat HZ, Abla O. Farah RA, et al. Mediterr J Hematol Infect Dis. 2015 Jan 1;7(1):e2015012. doi: 10.4084/MJHID.2015.012. eCollection 2015. Mediterr J Hematol Infect Dis. 2015. PMID: 25574371 Free PMC article.

3

A Novel Deletion in the RPL5 Gene in a Lebanese Child With Diamond Blackfan Anemia Unresponsive to Steroid Treatment.

Farah RA, Kamel L, Roy N, Proven M, Wray K, Roberts I, Wlodarski MW. Farah RA, et al. J Pediatr Hematol Oncol. 2020 May;42(4):e235-e237. doi: 10.1097/MPH.0000000000001435. J Pediatr Hematol Oncol. 2020. PMID: 30933022

4

Clinical phenotype, fibrinogen supplementation, and health-related quality of life in patients with afibrinogenemia.

Casini A, von Mackensen S, Santoro C, Djambas Khayat C, Belhani M, Ross C, Dorgalaleh A, Naz A, Ünal E, Abdelwahab M, Lozeron ED, Trillot N, Susen S, Peyvandi F, de Moerloose P; QualyAfib Study Group. Casini A, et al. Blood. 2021 Jun 3;137(22):3127-3136. doi: 10.1182/blood.2020009472. Blood. 2021. PMID: 33512441 Free article. Clinical Trial.

5

Acquired protein C deficiency in a child with acute myelogenous leukemia, splenic, renal, and intestinal infarction.

Farah RA, Jalkh KS, Farhat HZ, Sayad PE, Kadri AM. Farah RA, et al. Blood Coagul Fibrinolysis. 2011 Mar;22(2):140-3. doi: 10.1097/MBC.0b013e32834248e6. Blood Coagul Fibrinolysis. 2011. PMID: 21178585 Free article.

6

Ongoing issues with the management of children with Constitutional Mismatch Repair Deficiency syndrome.

Farah RA, Maalouf F, Chahine NA, Farhat H, Campbell B, Zhukova N, Durno C, Aronson M, Hawkins C, Bouffet E, Tabori U. Farah RA, et al. Eur J Med Genet. 2019 Aug;62(8):103706. doi: 10.1016/j.ejmg.2019.103706. Epub 2019 Jun 21. Eur J Med Genet. 2019. PMID: 31233827

7

Life-threatening bleeding in factor VII deficiency: the role of prenatal diagnosis and primary prophylaxis.

Farah R, Al Danaf J, Braiteh N, Costa JM, Farhat H, Mariani G, Giansily-Blaizot M. Farah R, et al. Br J Haematol. 2015 Feb;168(3):452-5. doi: 10.1111/bjh.13106. Epub 2014 Sep 2. Br J Haematol. 2015. PMID: 25179859 Free article. No abstract available.

8

Spontaneous epidural hematoma in a child with inherited factor XIII deficiency.

Farah RA, Al Danaf JZ, Chahinian RA, Braiteh NT, Al Ojaimi NF, Cairo A, Farhat H, Mantoura JR. Farah RA, et al. J Pediatr Hematol Oncol. 2014 Jan;36(1):62-5. doi: 10.1097/MPH.0b013e31828e52b6. J Pediatr Hematol Oncol. 2014. PMID: 23619114

9

Pandemic (H1N1) 2009 influenza in pediatric hematology/oncology units in Lebanon.

Noun P, Farah R, Bechara E, Hage P, Hajj MJ, Audi N, Khalifeh MC. Noun P, et al. Among authors: farah r. J Pediatr Hematol Oncol. 2013 Mar;35(2):144-7. doi: 10.1097/MPH.0b013e31827e4c68. J Pediatr Hematol Oncol. 2013. PMID: 23274382

10

Refractory autoimmune disease: an overview of when first-line therapy is not enough.

Neunert C, Farah R, Yacobovich J, Neufeld E. Neunert C, et al. Among authors: farah r. Semin Hematol. 2016 Apr;53 Suppl 1:S35-8. doi: 10.1053/j.seminhematol.2016.04.011. Epub 2016 Apr 7. Semin Hematol. 2016. PMID: 27312162 Review.

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