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Clinical Dysmorphology
|
December 1, 2011
TRPS1 codon 952 constitutes a mutational hot spot in trichorhinophalangeal syndrome type I and could be associated with intellectual disability
Jan A Sidler, Isabel Filges, Nemya Boesch, et al.
Pediatrics
|
January 11, 2012
Panhypopituitarism presenting as life-threatening heart failure caused by an inherited microdeletion in 1q25 including LHX4
Isabel Filges, Andrea Bischof-Renner, Benno Röthlisberger, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 8, 2004
Glucagon-like peptide 1 induces natriuresis in healthy subjects and in insulin-resistant obese men
Jean-Pierre Gutzwiller, Stefan Tschopp, Andreas Bock, et al.
Swiss Medical Weekly
|
December 2, 2009
Changes of coagulation parameters during high altitude expedition
Jacqueline Pichler Hefti, Lorenz Risch, Urs Hefti, et al.
British Journal of Haematology
|
January 27, 2024
Increased erythroferrone levels in malarial anaemia
Peter J Neyer, Bérenger Kaboré, Christos T Nakas, et al.
Malaria Journal
|
September 1, 2023
Exploring the host factors affecting asymptomatic Plasmodium falciparum infection: insights from a rural Burkina Faso study
Peter J Neyer, Bérenger Kaboré, Christos T Nakas, et al.
Gene
|
January 14, 2012
High resolution array in the clinical approach to chromosomal phenotypes
Isabel Filges, Luzia Suda, Peter Weber, et al.
High Altitude Medicine & Biology
|
September 27, 2013
Oxidative stress in hypobaric hypoxia and influence on vessel-tone modifying mediators
Jacqueline Pichler Hefti, Denise Sonntag, Urs Hefti, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 68) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 68 results.
Clinical Dysmorphology
|
December 1, 2011
TRPS1 codon 952 constitutes a mutational hot spot in trichorhinophalangeal syndrome type I and could be associated with intellectual disability
Jan A Sidler, Isabel Filges, Nemya Boesch, et al.
Pediatrics
|
January 11, 2012
Panhypopituitarism presenting as life-threatening heart failure caused by an inherited microdeletion in 1q25 including LHX4
Isabel Filges, Andrea Bischof-Renner, Benno Röthlisberger, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 8, 2004
Glucagon-like peptide 1 induces natriuresis in healthy subjects and in insulin-resistant obese men
Jean-Pierre Gutzwiller, Stefan Tschopp, Andreas Bock, et al.
Swiss Medical Weekly
|
December 2, 2009
Changes of coagulation parameters during high altitude expedition
Jacqueline Pichler Hefti, Lorenz Risch, Urs Hefti, et al.
British Journal of Haematology
|
January 27, 2024
Increased erythroferrone levels in malarial anaemia
Peter J Neyer, Bérenger Kaboré, Christos T Nakas, et al.
Malaria Journal
|
September 1, 2023
Exploring the host factors affecting asymptomatic Plasmodium falciparum infection: insights from a rural Burkina Faso study
Peter J Neyer, Bérenger Kaboré, Christos T Nakas, et al.
Gene
|
January 14, 2012
High resolution array in the clinical approach to chromosomal phenotypes
Isabel Filges, Luzia Suda, Peter Weber, et al.
High Altitude Medicine & Biology
|
September 27, 2013
Oxidative stress in hypobaric hypoxia and influence on vessel-tone modifying mediators
Jacqueline Pichler Hefti, Denise Sonntag, Urs Hefti, et al.
Page
of 7