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Journal of Internal Medicine
|
March 23, 2021
Early standardized clinical judgement for syncope diagnosis in the emergency department
J du Fay de Lavallaz, P Badertscher, T Zimmermann, et al.
Journal of Clinical Immunology
|
January 15, 2025
Hypomorphic RAG2 Deficiency Promotes Selection of Self-Reactive B Cells
Christopher D Thouvenel, Christopher M Tipton, Yasuhiro Yamazaki, et al.
Reports on Progress in Physics. Physical Society (Great Britain)
|
January 7, 2017
Attosecond physics at the nanoscale
M F Ciappina, J A Pérez-Hernández, A S Landsman, et al.
Neurological Research and Practice
|
December 16, 2020
S1 guidelines "lumbar puncture and cerebrospinal fluid analysis" (abridged and translated version)
H Tumani, H F Petereit, A Gerritzen, et al.
Acta Neuropathologica
|
October 5, 2020
Impairment of the mitochondrial one-carbon metabolism enzyme SHMT2 causes a novel brain and heart developmental syndrome
Àngels García-Cazorla, Edgard Verdura, Natalia Juliá-Palacios, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 27, 2021
Somatic PIK3R1 variation as a cause of vascular malformations and overgrowth
Catherine E Cottrell, Nicole R Bender, Michael T Zimmermann, et al.
The Lancet. Diabetes & Endocrinology
|
December 2, 2024
Treatment regimens and glycaemic outcomes in more than 100 000 children with type 1 diabetes (2013-22): a longitudinal analysis of data from paediatric diabetes registries
Anthony T Zimmermann, Stefanie Lanzinger, Siv Janne Kummernes, et al.
Fresenius' Journal of Analytical Chemistry
|
April 1, 2020
Bioluminescence, chemiluminescence
A Dwenger, C Beychok, G Schweitzer, et al.
Blood
|
May 19, 2019
Recurrent <i>MSC</i> <sup>E116K</sup> mutations in ALK-negative anaplastic large cell lymphoma
Rebecca A Luchtel, Michael T Zimmermann, Guangzhen Hu, et al.
American Journal of Human Genetics
|
May 11, 2023
Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy
Joel A Morales-Rosado, Tanya L Schwab, Sarah K Macklin-Mantia, et al.
Page
of 47
Search research articles
Search
Showing results (451-460 of 469) with videos related to
Sort By:
Page
of 47
Journal of Internal Medicine
|
March 23, 2021
Early standardized clinical judgement for syncope diagnosis in the emergency department
J du Fay de Lavallaz, P Badertscher, T Zimmermann, et al.
Journal of Clinical Immunology
|
January 15, 2025
Hypomorphic RAG2 Deficiency Promotes Selection of Self-Reactive B Cells
Christopher D Thouvenel, Christopher M Tipton, Yasuhiro Yamazaki, et al.
Reports on Progress in Physics. Physical Society (Great Britain)
|
January 7, 2017
Attosecond physics at the nanoscale
M F Ciappina, J A Pérez-Hernández, A S Landsman, et al.
Neurological Research and Practice
|
December 16, 2020
S1 guidelines "lumbar puncture and cerebrospinal fluid analysis" (abridged and translated version)
H Tumani, H F Petereit, A Gerritzen, et al.
Acta Neuropathologica
|
October 5, 2020
Impairment of the mitochondrial one-carbon metabolism enzyme SHMT2 causes a novel brain and heart developmental syndrome
Àngels García-Cazorla, Edgard Verdura, Natalia Juliá-Palacios, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 27, 2021
Somatic PIK3R1 variation as a cause of vascular malformations and overgrowth
Catherine E Cottrell, Nicole R Bender, Michael T Zimmermann, et al.
The Lancet. Diabetes & Endocrinology
|
December 2, 2024
Treatment regimens and glycaemic outcomes in more than 100 000 children with type 1 diabetes (2013-22): a longitudinal analysis of data from paediatric diabetes registries
Anthony T Zimmermann, Stefanie Lanzinger, Siv Janne Kummernes, et al.
Fresenius' Journal of Analytical Chemistry
|
April 1, 2020
Bioluminescence, chemiluminescence
A Dwenger, C Beychok, G Schweitzer, et al.
Blood
|
May 19, 2019
Recurrent <i>MSC</i> <sup>E116K</sup> mutations in ALK-negative anaplastic large cell lymphoma
Rebecca A Luchtel, Michael T Zimmermann, Guangzhen Hu, et al.
American Journal of Human Genetics
|
May 11, 2023
Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy
Joel A Morales-Rosado, Tanya L Schwab, Sarah K Macklin-Mantia, et al.
Page
of 47