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Innere Medizin (Heidelberg, Germany)
|
May 21, 2024
[Heritable pulmonary arterial hypertension]
Christina A Eichstaedt, Memoona Shaukat, Ekkehard Grünig
European Journal of Medical Genetics
|
September 16, 2019
RIN2 and BBS7 variants as cause of a coincidental syndrome
Memoona Shaukat, Tayyaba Ishaq, Niaz Muhammad, et al.
Current Opinion in Pulmonary Medicine
|
June 24, 2024
Genetic background of pulmonary (vascular) diseases - how much is written in the codes?
Christina A Eichstaedt, Simon O Haas, Memoona Shaukat, et al.
Journal of Medical Virology
|
August 23, 2018
The implication of CRISPR/Cas9 genome editing technology in combating human oncoviruses
Usman Gilani, Memoona Shaukat, Arisha Rasheed, et al.
Respiratory Research
|
November 10, 2021
Prognostic impact of hypochromic erythrocytes in patients with pulmonary arterial hypertension
Panagiota Xanthouli, Vivienne Theobald, Nicola Benjamin, et al.
Scientific Reports
|
January 29, 2026
Heritable pulmonary arterial hypertension: new genetic findings and environmental triggers
Memoona Shaukat, Ekkehard Grünig, Simon Haas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 9, 2023
Defining the clinical validity of genes reported to cause pulmonary arterial hypertension
Carrie L Welch, Micheala A Aldred, Srimmitha Balachandar, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 9, 2024
Adaptation of ACMG/AMP guidelines for clinical classification of <i>BMPR2</i> variants in Pulmonary Arterial Hypertension resolves variants of unclear pathogenicity in ClinVar
Christina A Eichstaedt, Gabriel Maldonado-Velez, Rajiv D Machado, et al.
Human Mutation
|
July 15, 2025
Adaptation of ACMG/AMP Guidelines for Clinical Classification of <i>BMPR2</i> Variants in Pulmonary Arterial Hypertension Resolves Variants of Unclear Pathogenicity in ClinVar
Christina A Eichstaedt, Gabriel Maldonado-Velez, Rajiv D Machado, et al.
NPJ Genomic Medicine
|
March 26, 2025
Pathogenic SMAD6 variants in patients with idiopathic and complex congenital heart disease associated pulmonary arterial hypertension
Sofia Karl, Ekkehard Grünig, Memoona Shaukat, et al.
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Search research articles
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Showing results (1-10 of 11) with videos related to
Sort By:
Page
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Innere Medizin (Heidelberg, Germany)
|
May 21, 2024
[Heritable pulmonary arterial hypertension]
Christina A Eichstaedt, Memoona Shaukat, Ekkehard Grünig
European Journal of Medical Genetics
|
September 16, 2019
RIN2 and BBS7 variants as cause of a coincidental syndrome
Memoona Shaukat, Tayyaba Ishaq, Niaz Muhammad, et al.
Current Opinion in Pulmonary Medicine
|
June 24, 2024
Genetic background of pulmonary (vascular) diseases - how much is written in the codes?
Christina A Eichstaedt, Simon O Haas, Memoona Shaukat, et al.
Journal of Medical Virology
|
August 23, 2018
The implication of CRISPR/Cas9 genome editing technology in combating human oncoviruses
Usman Gilani, Memoona Shaukat, Arisha Rasheed, et al.
Respiratory Research
|
November 10, 2021
Prognostic impact of hypochromic erythrocytes in patients with pulmonary arterial hypertension
Panagiota Xanthouli, Vivienne Theobald, Nicola Benjamin, et al.
Scientific Reports
|
January 29, 2026
Heritable pulmonary arterial hypertension: new genetic findings and environmental triggers
Memoona Shaukat, Ekkehard Grünig, Simon Haas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 9, 2023
Defining the clinical validity of genes reported to cause pulmonary arterial hypertension
Carrie L Welch, Micheala A Aldred, Srimmitha Balachandar, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 9, 2024
Adaptation of ACMG/AMP guidelines for clinical classification of <i>BMPR2</i> variants in Pulmonary Arterial Hypertension resolves variants of unclear pathogenicity in ClinVar
Christina A Eichstaedt, Gabriel Maldonado-Velez, Rajiv D Machado, et al.
Human Mutation
|
July 15, 2025
Adaptation of ACMG/AMP Guidelines for Clinical Classification of <i>BMPR2</i> Variants in Pulmonary Arterial Hypertension Resolves Variants of Unclear Pathogenicity in ClinVar
Christina A Eichstaedt, Gabriel Maldonado-Velez, Rajiv D Machado, et al.
NPJ Genomic Medicine
|
March 26, 2025
Pathogenic SMAD6 variants in patients with idiopathic and complex congenital heart disease associated pulmonary arterial hypertension
Sofia Karl, Ekkehard Grünig, Memoona Shaukat, et al.
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of 2