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Clinical Genetics
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December 18, 2019
VPS26C homozygous nonsense variant in two cousins with neurodevelopmental deficits, growth failure, skeletal abnormalities, and distinctive facial features
Christian Beetz, Najim Ameziane, Ameni Kdissa, et al.
Scientific Reports
|
May 26, 2023
Nationwide analysis of hospital admissions and outcomes of patients with SARS-CoV-2 infection in Austria in 2020 and 2021
Paul Zajic, Michael Hiesmayr, Peter Bauer, et al.
Parkinsonism & Related Disorders
|
May 3, 2014
Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: a novel entity?
Klas Wictorin, Björn Brådvik, Karin Nilsson, et al.
Bioanalysis
|
February 4, 2022
Quantitation of a plasma biomarker profile for the early detection of Gaucher disease type 1 patients
Iskren Menkovic, Michel Boutin, Abdulfatah Alayoubi, et al.
Critical Care (London, England)
|
September 8, 2017
Weekends affect mortality risk and chance of discharge in critically ill patients: a retrospective study in the Austrian registry for intensive care
Paul Zajic, Peter Bauer, Andrew Rhodes, et al.
Philosophical Transactions. Series A, Mathematical, Physical, and Engineering Sciences
|
April 11, 2019
Assessing the scales in numerical weather and climate predictions: will exascale be the rescue?
Philipp Neumann, Peter Düben, Panagiotis Adamidis, et al.
Annals of Neurology
|
July 3, 2003
Do CTG expansions at the SCA8 locus cause ataxia?
Ludger Schöls, Ingrid Bauer, Christine Zühlke, et al.
Parkinsonism & Related Disorders
|
October 13, 2020
Intermediate phenotype of ATP13A2 mutation in two Chilean siblings: Towards a continuum between parkinsonism and hereditary spastic paraplegia
Marcelo Miranda, Florian Harmuth, M Leonor Bustamante, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 1, 2022
How relevant are cerebral white matter lesions in the D313Y variant of the α-galactosidase A gene? Neurological, cardiological, laboratory, and MRI data of 21 patients within a follow-up of 3 years
Daniel Strunk, Jana Becker, Roland Veltkamp, et al.
European Journal of Anaesthesiology
|
May 6, 2011
EuSOS: European surgical outcomes study
Rupert M Pearse, Andrew Rhodes, Rui Moreno, et al.
Page
of 59
Search research articles
Search
Showing results (171-180 of 585) with videos related to
Sort By:
Page
of 59
Clinical Genetics
|
December 18, 2019
VPS26C homozygous nonsense variant in two cousins with neurodevelopmental deficits, growth failure, skeletal abnormalities, and distinctive facial features
Christian Beetz, Najim Ameziane, Ameni Kdissa, et al.
Scientific Reports
|
May 26, 2023
Nationwide analysis of hospital admissions and outcomes of patients with SARS-CoV-2 infection in Austria in 2020 and 2021
Paul Zajic, Michael Hiesmayr, Peter Bauer, et al.
Parkinsonism & Related Disorders
|
May 3, 2014
Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: a novel entity?
Klas Wictorin, Björn Brådvik, Karin Nilsson, et al.
Bioanalysis
|
February 4, 2022
Quantitation of a plasma biomarker profile for the early detection of Gaucher disease type 1 patients
Iskren Menkovic, Michel Boutin, Abdulfatah Alayoubi, et al.
Critical Care (London, England)
|
September 8, 2017
Weekends affect mortality risk and chance of discharge in critically ill patients: a retrospective study in the Austrian registry for intensive care
Paul Zajic, Peter Bauer, Andrew Rhodes, et al.
Philosophical Transactions. Series A, Mathematical, Physical, and Engineering Sciences
|
April 11, 2019
Assessing the scales in numerical weather and climate predictions: will exascale be the rescue?
Philipp Neumann, Peter Düben, Panagiotis Adamidis, et al.
Annals of Neurology
|
July 3, 2003
Do CTG expansions at the SCA8 locus cause ataxia?
Ludger Schöls, Ingrid Bauer, Christine Zühlke, et al.
Parkinsonism & Related Disorders
|
October 13, 2020
Intermediate phenotype of ATP13A2 mutation in two Chilean siblings: Towards a continuum between parkinsonism and hereditary spastic paraplegia
Marcelo Miranda, Florian Harmuth, M Leonor Bustamante, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 1, 2022
How relevant are cerebral white matter lesions in the D313Y variant of the α-galactosidase A gene? Neurological, cardiological, laboratory, and MRI data of 21 patients within a follow-up of 3 years
Daniel Strunk, Jana Becker, Roland Veltkamp, et al.
European Journal of Anaesthesiology
|
May 6, 2011
EuSOS: European surgical outcomes study
Rupert M Pearse, Andrew Rhodes, Rui Moreno, et al.
Page
of 59