S. Al-Tamemi

发表

Extended-spectrum β-lactamase (ESBL) in Omani Children: Study of prevalence, risk factors and clinical outcomes at Sultan Qaboos University Hospital, Sultanate of Oman.

A. Balkhair, A. Rafay, Zakariya Al Muharrmi, 2008, Sultan Qaboos University medical journal.

The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.

A. Schäffer, V. Lougaris, R. Geha, 2015, The Journal of allergy and clinical immunology.

DOCK8 is essential for LFA-1 dependent positioning of T follicular helper cells in germinal centers.

F. Luscinskas, R. Geha, E. Janssen, 2020, JCI insight.

Combined Immunodeficiency, Hemolytic Anemia, and Growth Retardation Secondary to a Homozygous Mutation in the NHEJ1 Gene.

Y. Wali, S. Naseem, S. Al-Tamemi, 2020, Journal of pediatric hematology/oncology.

Combined immunodeficiency due to a mutation in the γ1 subunit of the coat protein I complex.

J. Orange, R. Geha, J. Chou, 2021, The Journal of clinical investigation.

BCG Vaccine–associated Complications in a Large Cohort of Children With Combined Immunodeficiencies Affecting Cellular and Humoral Immunity

W. Al-Herz, M. Al-Nesf, S. Al-Hammadi, 2022, The Pediatric infectious disease journal.

Food Allergen Sensitisation Patterns in Omani Patients with Allergic Manifestations.

S. Naseem, S. Al-Tamemi, Mahmood Al-Kindi, 2019, Sultan Qaboos University medical journal.

Primary Immunodeficiency Diseases in Oman: 10-Year Experience in a Tertiary Care Hospital

A. Al-Rawas, S. Naseem, S. Al-Tamemi, 2016, Journal of Clinical Immunology.

BCG vaccination in patients with severe combined immunodeficiency: complications, risks, and vaccination policies.

J. Franco, W. Al-Herz, T. Morio, 2014, The Journal of allergy and clinical immunology.

Immune supplementation and immune modulation with intravenous immunoglobulin.

Q. Hamid, B. Mazer, S. Al-Tamemi, 2005, The Journal of allergy and clinical immunology.

Consensus on diagnosis and management of Hereditary Angioedema in the Middle East: A Delphi initiative

W. Al-Herz, M. Al-Ahmad, M. Abuzakouk, 2022, The World Allergy Organization journal.

An intronic mutation in DKC1 in an infant with Høyeraal–Hreidarsson syndrome

A. Al-Eyadhy, S. Bale, S. Abish, 2008, American journal of medical genetics. Part A.

Acute Idiopathic Pulmonary Haemorrhage in a 2 month old Infant: Case report and review of the literature.

S. Al-Tamemi, H. Al-Kindi, 2009, Sultan Qaboos University medical journal.

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome.

Edward R B McCabe, Bodo Grimbacher, Christoph Klein, 2009, The Journal of allergy and clinical immunology.

Correlation between flow cytometry and molecular findings in autosomal recessive chronic granulomatous disease: A cohort study from Oman

S. Al-Mamari, S. Al-Tamemi, A. Al-Riyami, 2018, International journal of laboratory hematology.

Combined immunodeficiency due to a homozygous mutation in ORAI1 that deletes the C-terminus that interacts with STIM 1.

R. Geha, J. Chou, M. Massaad, 2016, Clinical immunology.

Clinical and molecular findings of chronic granulomatous disease in Oman: family studies

A. Pathare, R. Krishnamoorthy, C. Lapouméroulie, 2015, Clinical genetics.

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome.

T. Chatila, S. Holland, C. Klein, 2009, The Journal of allergy and clinical immunology.

Unilateral Tongue Angioedema Induced by Angiotensin Converting Enzyme Inhibitor: A Case Report

S. Al-Tamemi, A. Al-Mahrezi, Maisa Hamed Al-Kiyumi, 2020, Oman medical journal.

Chediak-Higashi Syndrome: Novel Mutation of the CHS1/LYST Gene in 3 Omani Patients

S. Al-Tamemi, D. Dennison, S. Al-Zadjali, 2014, Journal of pediatric hematology/oncology.

Genetic Causes, Clinical Features, and Survival of Underlying Inborn Errors of Immunity in Omani Patients: a Single-Center Study

Z. Bruwer, A. Al-Maawali, S. Naseem, 2022, Journal of Clinical Immunology.

BCL10 loss-of-function novel mutation leading to atypical severe combined immunodeficiency.

A. Al-Maawali, S. Al-Tamemi, Mahmood Al-Kindi, 2022, Clinical immunology.

Consensus Middle East and North Africa Registry on Inborn Errors of Immunity

R. Geha, A. Bousfiha, W. Al-Herz, 2021, Journal of Clinical Immunology.

Pearson's Marrow-Pancreas Syndrome.

S. Al-Tamemi, 2009, Sultan Qaboos University medical journal.

Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry.

R. Geha, J. Chou, W. Al-Herz, 2022, Clinical immunology.

Primary Immunodeficiency Diseases in Oman: Five Years' Experience at Sultan Qaboos University Hospital

I. Elnour, S. Al-Tamemi, D. Dennison, 2012, The World Allergy Organization journal.

Predictors of early death risk among untransplanted patients with combined immunodeficiencies affecting cellular and humoral immunity: A multicenter report

W. Al-Herz, M. Al-Nesf, A. Ziyab, 2022, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Complete DiGeorge Anomaly in the Absence of Neonatal Hypocalcemia and Velofacial and Cardiac Defects

N. Jabado, A. Duncan, B. Mazer, 2005, Pediatrics.

Semaphorin 4C: A Novel Component of B-Cell Polarization in Th2-Driven Immune Responses

R. Friedel, B. Mazer, W. Mourad, 2016, Frontiers in immunology.

Semaphorin 4C: A Novel Component of B-Cell Polarization in Th2-Driven Immune Responses

R. Friedel, B. Mazer, W. Mourad, 2016, Front. Immunol..

The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity.

R. Geha, A. Bousfiha, W. Al-Herz, 2022, The journal of allergy and clinical immunology. In practice.

The pattern of sensitisation to inhalant allergens in omani patients with asthma, allergic rhinitis and rhinoconjunctivitis.

R. Al-Abri, O. Al-Rawas, B. Al-Riyami, 2008, Sultan Qaboos University medical journal.

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome (vol 124, pg 1289, 2009)

T. Chatila, J. Puck, S. Ehl, 2010 .

COVID-19 Vaccination in Patients with Inborn Errors of Immunity Reduces Hospitalization and Critical Care Needs Related to COVID-19: a USIDNET Report

G. Giardino, C. Pignata, J. Puck, 2024, Journal of clinical immunology.

Immune reconstitution and survival, following hematopoietic stem cell transplantation in Omani patients with inborn errors of immunity

M. Al-Khabori, S. Al-Tamemi, K. al-Farsi, 2024, Clinical Immunology.

Epidemiology of combined immunodeficiencies affecting cellular and humoral immunity- A multicentric retrospective cohort study from the Arabian Peninsula.

W. Al-Herz, M. Al-Nesf, A. Ziyab, 2023, Clinical immunology.