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Orphanet Journal of Rare Diseases
|
April 18, 2024
Pregnancy outcomes of Fabry disease in Austria (PROFABIA)-a retrospective cohort-study
Natalja Haninger-Vacariu, Kyra Anastopoulos, Christof Aigner, et al.
Gene
|
June 5, 2013
CYP2C9 genotype and association with bone mineral density: a pilot study
Sophie Brunner-Ziegler, Georgiana-Aura Giurgea, Raute Sunder-Plassmann, et al.
Pediatric Blood & Cancer
|
June 24, 2023
Dominant inherited β-thalassemia intermedia in a Polish family due to a novel frameshift mutation in HBB
Wolfgang Novak, Raute Sunder-Plassmann, Jakob Berner, et al.
International Journal of Medical Sciences
|
May 27, 2016
Screening for Fabry Disease by Urinary Globotriaosylceramide Isoforms Measurement in Patients with Left Ventricular Hypertrophy
Martina Gaggl, Natalija Lajic, Georg Heinze, et al.
European Journal of Preventive Cardiology
|
November 13, 2024
Performance of LDL-C only compared to the Dutch Lipid Clinic Network Score for screening of familial hypercholesterolaemia: the Austrian experience and literature review
Moritz Ferch, Lukas Galli, Paul Fellinger, et al.
Clinical Kidney Journal
|
April 12, 2021
Pregnancies in kidney transplant recipients with complement gene variant-mediated thrombotic microangiopathy
Natalja Haninger-Vacariu, Christof Aigner, Martina Gaggl, et al.
Kidney & Blood Pressure Research
|
October 22, 2024
New-Onset Complement-Mediated Thrombotic Microangiopathy during the COVID-19 Pandemic
Christof Aigner, Martina Gaggl, Sophie Schmidt, et al.
Kidney International Reports
|
June 26, 2023
Complement-Mediated Thrombotic Microangiopathy Related to COVID-19 or SARS-CoV-2 Vaccination
Christof Aigner, Martina Gaggl, Sophie Schmidt, et al.
JAMA Dermatology
|
February 22, 2013
Identification of a homozygous PSTPIP1 mutation in a patient with a PAPA-like syndrome responding to canakinumab treatment
Alexandra Geusau, Nadine Mothes-Luksch, Hesam Nahavandi, et al.
Case Reports in Transplantation
|
May 22, 2013
A single lung transplant in a patient with fabry disease: causality or far-fetched? A case report
Martina Gaggl, Renate Kain, Peter Jaksch, et al.
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Search research articles
Search
Showing results (21-30 of 53) with videos related to
Sort By:
Page
of 6
Orphanet Journal of Rare Diseases
|
April 18, 2024
Pregnancy outcomes of Fabry disease in Austria (PROFABIA)-a retrospective cohort-study
Natalja Haninger-Vacariu, Kyra Anastopoulos, Christof Aigner, et al.
Gene
|
June 5, 2013
CYP2C9 genotype and association with bone mineral density: a pilot study
Sophie Brunner-Ziegler, Georgiana-Aura Giurgea, Raute Sunder-Plassmann, et al.
Pediatric Blood & Cancer
|
June 24, 2023
Dominant inherited β-thalassemia intermedia in a Polish family due to a novel frameshift mutation in HBB
Wolfgang Novak, Raute Sunder-Plassmann, Jakob Berner, et al.
International Journal of Medical Sciences
|
May 27, 2016
Screening for Fabry Disease by Urinary Globotriaosylceramide Isoforms Measurement in Patients with Left Ventricular Hypertrophy
Martina Gaggl, Natalija Lajic, Georg Heinze, et al.
European Journal of Preventive Cardiology
|
November 13, 2024
Performance of LDL-C only compared to the Dutch Lipid Clinic Network Score for screening of familial hypercholesterolaemia: the Austrian experience and literature review
Moritz Ferch, Lukas Galli, Paul Fellinger, et al.
Clinical Kidney Journal
|
April 12, 2021
Pregnancies in kidney transplant recipients with complement gene variant-mediated thrombotic microangiopathy
Natalja Haninger-Vacariu, Christof Aigner, Martina Gaggl, et al.
Kidney & Blood Pressure Research
|
October 22, 2024
New-Onset Complement-Mediated Thrombotic Microangiopathy during the COVID-19 Pandemic
Christof Aigner, Martina Gaggl, Sophie Schmidt, et al.
Kidney International Reports
|
June 26, 2023
Complement-Mediated Thrombotic Microangiopathy Related to COVID-19 or SARS-CoV-2 Vaccination
Christof Aigner, Martina Gaggl, Sophie Schmidt, et al.
JAMA Dermatology
|
February 22, 2013
Identification of a homozygous PSTPIP1 mutation in a patient with a PAPA-like syndrome responding to canakinumab treatment
Alexandra Geusau, Nadine Mothes-Luksch, Hesam Nahavandi, et al.
Case Reports in Transplantation
|
May 22, 2013
A single lung transplant in a patient with fabry disease: causality or far-fetched? A case report
Martina Gaggl, Renate Kain, Peter Jaksch, et al.
Page
of 6