Resultados de procura - Abdulrahman Alsultan
- Mostrando 1 - 11 Resultados de 11
-
1
-
2
-
3
-
4
High frequency of carbapenem-resistant Acinetobacter baumannii in patients with diabetes mellitus in Saudi Arabia por Abdulrahman Alsultan, Benjamin A. Evans, Elsayed A. Elsayed, Sahar Althawadi, Abdulla Al‐Taher, S. G. B. Amyes, A.M. AL-Dughaym, Ahmed Hamouda
Publicado 2013Artigo -
5
LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency por Abdullah Alangari, Abdulrahman Alsultan, Nouran Adly, Michel J. Massaad, Iram Shakir Kiani, Abdulrahman Aljebreen, Emad Raddaoui, Abdulkareem Al-Momen, Saleh Al‐Muhsen, Raif S. Geha, Fowzan S. Alkuraya
Publicado 2012Artigo -
6
Sickle cell disease in <scp>S</scp>audi <scp>A</scp>rabia: the phenotype in adults with the <scp>A</scp>rab‐<scp>I</scp>ndian haplotype is not benign por Abdulrahman Alsultan, Mohammed K. Alabdulaali, Paula J. Griffin, Ahmed Alsuliman, Hazem A. Ghabbour, Paola Sebastiani, Waleed H. Albuali, Amein K. Al‐Ali, David H.K. Chui, Martin H. Steinberg
Publicado 2013Artigo -
7
A phased SNP-based classification of sickle cell anemia HBB haplotypes por Elmutaz Shaikho Elhaj Mohammed, John J. Farrell, Abdulrahman Alsultan, Hatem Qutub, Amein K. Al‐Ali, Maria Stella Figueiredo, David H.K. Chui, Lindsay A. Farrer, George J. Murphy, Gustavo Mostoslavsky, Paola Sebastiani, Martin H. Steinberg
Publicado 2017Artigo -
8
Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked–like disorder caused by loss-of-function mutations in LRBA por Louis‐Marie Charbonnier, Erin Janssen, Janet Chou, Toshiro K. Ohsumi, Sevgi Keleş, Joyce T. Hsu, Michel J. Massaad, Maria Garcia-Lloret, Rima Hanna‐Wakim, Ghassan Dbaibo, Abdullah Alangari, Abdulrahman Alsultan, Daifulah Al-Zahrani, Raif S. Geha, Talal A. Chatila
Publicado 2014Artigo -
9
Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype por Duyen Ngo, Harold Bae, Martin H. Steinberg, Paola Sebastiani, Nadia Solovieff, Clinton T. Baldwin, Efthymia Melista, Surinder Safaya, Lindsay A. Farrer, Ahmed Alsuliman, Waleed H. Albuali, Muneer H. Al Bagshi, Zaki A. Naserullah, Idowu Akinsheye, Patrick G. Gallagher, Hongyuan Luo, David H.K. Chui, John Farrell, Amein K. Al‐Ali, Abdulrahman Alsultan
Publicado 2013Artigo -
10
Effective treatment of steroid and therapy-refractory acute graft-versus-host disease with a novel mesenchymal stromal cell product (MSC-FFM) por Peter Bader, Zyrafete Kuçi, Shahrzad Bakhtiar, Oliver Basu, Gesine Bug, Michael Dennis, Johann Greil, Anikó Barta, Krisztián Kállay, Peter Lang, Giovanna Lucchini, Raj Pol, Ansgar Schulz, Karl‐Walter Sykora, Irene von Luettichau, Grit S. Herter-Sprie, Mohammad Ashab Uddin, Phil Jenkin, Abdulrahman Alsultan, Jochen Buechner, Jerry Stein, Ágnes Kelemen, Andrea Jarisch, Jan Soerensen, Emilia Salzmann‐Manrique, Martin Hutter, Richard Schäfer, Erhard Seifried, Thomas Klingebiel, Halvard Bönig, Selim Kuçi
Publicado 2018Artigo -
11
Children and Adults with Refractory Acute Graft-versus-Host Disease Respond to Treatment with the Mesenchymal Stromal Cell Preparation “MSC-FFM”—Outcome Report of 92 Patients por Halvard Bönig, Zyrafete Kuçi, Selim Kuçi, Shahrzad Bakhtiar, Oliver Basu, Gesine Bug, Mike Dennis, Johann Greil, Anikó Barta, Krisztián Kállay, Peter Lang, Giovanna Lucchini, Raj Pol, Ansgar Schulz, Karl‐Walter Sykora, Irene Teichert von Luettichau, Grit S. Herter-Sprie, Mohammad Ashab Uddin, Phil Jenkin, Abdulrahman Alsultan, Jochen Buechner, Jerry Stein, Ágnes Kelemen, Andrea Jarisch, Jan Soerensen, Emilia Salzmann‐Manrique, Martin Hutter, Richard Schäfer, Erhard Seifried, Shankara Paneesha, Igor Novitzky‐Basso, Aharon Gefen, Neta Nevo, Gernot Beutel, Paul‐Gerhardt Schlegel, Thomas Klingebiel, Peter Bader
Publicado 2019Artigo
Ferramentas de procura:
Materias Relacionadas
Medicine
Internal medicine
Biology
Genetics
Gene
Disease
Immunology
Sickle cell anemia
Haplotype
Anemia
Cell
Fetal hemoglobin
Fetus
Gastroenterology
Genotype
Pathology
Pregnancy
Acute chest syndrome
Antibody
Astrobiology
Bone marrow
Common variable immunodeficiency
Hemoglobin
Hemoglobinopathy
Immune dysregulation
Immune system
Mesenchymal stem cell
Mutation
Physics
Primary immunodeficiency