Author/Creator: Marzouk, Iman - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Marzouk, Iman

1. Hyperimmunoglobulinemia and IgG Subclass Abnormalities in Children With Gaucher Disease. Issue 7 (October 2019)

Authors:: Marzouk, Iman; Deghady, Akram; Omar, Omneya M.; Ashour, Rofaida S.
Journal:: Journal of pediatric hematology/oncology
Issue:: Volume 41:Issue 7(2019)
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Record Type:: Journal Article
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2. Mutations in ALDH1A3 Represent a Frequent Cause of Microphthalmia/Anophthalmia in Consanguineous Families. Issue 8 (3rd June 2014)

Authors:: Abouzeid, Hana; Favez, Tatiana; Schmid, Angélique; Agosti, Céline; Youssef, Mohammed; Marzouk, Iman; El Shakankiry, Nihal; Bayoumi, Nader; Munier, Francis L.; Schorderet, Daniel F.
Journal:: Human mutation
Issue:: Volume 35:Issue 8(2014:Aug.)
Page Start:: 949
Record Type:: Journal Article
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3. Results From a 12-Month Open-Label Phase 1/2 Study of Velaglucerase Alfa in Children and Adolescents With Type 3 Gaucher Disease. (12th April 2018)

Authors:: Tantawy, Azza A. G.; El-Beshlawy, Amal; Marzouk, Iman; Bavdekar, Ashish; Qin, Yulin; Mellgard, Björn; Ben Turkia, Hadhami
Journal:: Journal of inborn errors of metabolism and screening
Issue:: Volume 6(2018)
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Record Type:: Journal Article
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