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The European Respiratory Journal
|
November 9, 2016
Pulmonary arteriovenous malformations: an uncharacterised phenotype of dyskeratosis congenita and related telomere biology disorders
Payal P Khincha, Alison A Bertuch, Suneet Agarwal, et al.
Haematologica
|
April 4, 2020
Genotype-phenotype association and variant characterization in Diamond-Blackfan anemia caused by pathogenic variants in <i>RPL35A</i>
Matthew D Gianferante, Marcin W Wlodarski, Evangelia Atsidaftos, et al.
Respiratory Research
|
January 24, 2024
Midregional proatrial naturetic peptide (MRproANP) and copeptin (COPAVP) as predictors of all-cause mortality in recently diagnosed mild to moderate COPD-results from COSYCONET
S Fähndrich, C Herr, S Teuteberg, et al.
Plos Genetics
|
September 7, 2013
A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome
Bari J Ballew, Vijai Joseph, Saurav De, et al.
Respiratory Research
|
May 15, 2024
Statins did not reduce the frequency of exacerbations in individuals with COPD and cardiovascular comorbidities in the COSYCONET cohort
N Frantzi, X P Nguyen, C Herr, et al.
Science Translational Medicine
|
October 22, 2020
Calmodulin inhibitors improve erythropoiesis in Diamond-Blackfan anemia
Alison M Taylor, Elizabeth R Macari, Iris T Chan, et al.
The Journal of Pediatrics
|
November 5, 2011
Extended spectrum of human glucose-6-phosphatase catalytic subunit 3 deficiency: novel genotypes and phenotypic variability in severe congenital neutropenia
Kaan Boztug, Philip S Rosenberg, Marie Dorda, et al.
Science Translational Medicine
|
February 10, 2017
Drug discovery for Diamond-Blackfan anemia using reprogrammed hematopoietic progenitors
Sergei Doulatov, Linda T Vo, Elizabeth R Macari, et al.
The Journal of Pediatrics
|
September 24, 2020
Gastrointestinal Hemorrhage: A Manifestation of the Telomere Biology Disorders
Ryan W Himes, Eric H Chiou, Karen Queliza, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation
|
June 28, 2015
Second Allogeneic Hematopoietic Cell Transplantation for Patients with Fanconi Anemia and Bone Marrow Failure
Mouhab Ayas, Mary Eapen, Jennifer Le-Rademacher, et al.
Page
of 37
Search research articles
Search
Showing results (341-350 of 362) with videos related to
Sort By:
Page
of 37
The European Respiratory Journal
|
November 9, 2016
Pulmonary arteriovenous malformations: an uncharacterised phenotype of dyskeratosis congenita and related telomere biology disorders
Payal P Khincha, Alison A Bertuch, Suneet Agarwal, et al.
Haematologica
|
April 4, 2020
Genotype-phenotype association and variant characterization in Diamond-Blackfan anemia caused by pathogenic variants in <i>RPL35A</i>
Matthew D Gianferante, Marcin W Wlodarski, Evangelia Atsidaftos, et al.
Respiratory Research
|
January 24, 2024
Midregional proatrial naturetic peptide (MRproANP) and copeptin (COPAVP) as predictors of all-cause mortality in recently diagnosed mild to moderate COPD-results from COSYCONET
S Fähndrich, C Herr, S Teuteberg, et al.
Plos Genetics
|
September 7, 2013
A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome
Bari J Ballew, Vijai Joseph, Saurav De, et al.
Respiratory Research
|
May 15, 2024
Statins did not reduce the frequency of exacerbations in individuals with COPD and cardiovascular comorbidities in the COSYCONET cohort
N Frantzi, X P Nguyen, C Herr, et al.
Science Translational Medicine
|
October 22, 2020
Calmodulin inhibitors improve erythropoiesis in Diamond-Blackfan anemia
Alison M Taylor, Elizabeth R Macari, Iris T Chan, et al.
The Journal of Pediatrics
|
November 5, 2011
Extended spectrum of human glucose-6-phosphatase catalytic subunit 3 deficiency: novel genotypes and phenotypic variability in severe congenital neutropenia
Kaan Boztug, Philip S Rosenberg, Marie Dorda, et al.
Science Translational Medicine
|
February 10, 2017
Drug discovery for Diamond-Blackfan anemia using reprogrammed hematopoietic progenitors
Sergei Doulatov, Linda T Vo, Elizabeth R Macari, et al.
The Journal of Pediatrics
|
September 24, 2020
Gastrointestinal Hemorrhage: A Manifestation of the Telomere Biology Disorders
Ryan W Himes, Eric H Chiou, Karen Queliza, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation
|
June 28, 2015
Second Allogeneic Hematopoietic Cell Transplantation for Patients with Fanconi Anemia and Bone Marrow Failure
Mouhab Ayas, Mary Eapen, Jennifer Le-Rademacher, et al.
Page
of 37