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BMC Musculoskeletal Disorders
|
April 6, 2013
The role of the combination of bone and fall related risk factors on short-term subsequent fracture risk and mortality
Kirsten M B Huntjens, Tineke A C M van Geel, Svenhjalmar van Helden, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Molecular genetics of facioscapulohumeral muscular dystrophy
C Wijmenga, R R Frants, J E Hewitt, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)
|
August 7, 2009
Identification of a recurrent mutation in the protoporphyrinogen oxidase gene in Swiss patients with variegate porphyria: clinical and genetic implications
A M Van Tuyll Van Serooskerke, X Schneider-Yin, R J Schimmel, et al.
American Journal of Human Genetics
|
January 1, 1995
Spectrum of mutations in the gene encoding the adrenoleukodystrophy protein
M J Ligtenberg, S Kemp, C O Sarde, et al.
Clinical Lung Cancer
|
June 19, 2025
Osimertinib Dose Optimization Guided by Therapeutic Drug Monitoring in Patients With EGFR-Mutated Advanced Non-Small Cell Lung Cancer: A Case series
Paul D Kruithof, Anita J W M Brouns, Juliette H R J Degens, et al.
European Respiratory Review : an Official Journal of the European Respiratory Society
|
June 15, 2022
Practical recommendations to combine small-molecule inhibitors and direct oral anticoagulants in patients with nonsmall cell lung cancer
Leila S Otten, Berber Piet, Michel M van den Heuvel, et al.
Maturitas
|
September 7, 2014
Increased fracture risk in patients with type 2 diabetes mellitus: an overview of the underlying mechanisms and the usefulness of imaging modalities and fracture risk assessment tools
Ellis A C de Waard, Tineke A C M van Geel, Hans H C M Savelberg, et al.
Platelets
|
June 24, 2006
Lorenzo's oil and platelet activation in adrenomyeloneuropathy and asymptomatic X-linked adrenoleukodystrophy
A Konijnenberg, B M van Geel, A Sturk, et al.
Biochemical and Biophysical Research Communications
|
July 29, 1994
Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutations
S Kemp, M J Ligtenberg, B M van Geel, et al.
Journal of the Peripheral Nervous System : JPNS
|
December 20, 2011
X-linked adrenomyeloneuropathy due to a novel missense mutation in the ABCD1 start codon presenting as demyelinating neuropathy
Marc Engelen, Anneke J van der Kooi, Stephan Kemp, et al.
Page
of 18
Search research articles
Search
Showing results (101-110 of 172) with videos related to
Sort By:
Page
of 18
BMC Musculoskeletal Disorders
|
April 6, 2013
The role of the combination of bone and fall related risk factors on short-term subsequent fracture risk and mortality
Kirsten M B Huntjens, Tineke A C M van Geel, Svenhjalmar van Helden, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Molecular genetics of facioscapulohumeral muscular dystrophy
C Wijmenga, R R Frants, J E Hewitt, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)
|
August 7, 2009
Identification of a recurrent mutation in the protoporphyrinogen oxidase gene in Swiss patients with variegate porphyria: clinical and genetic implications
A M Van Tuyll Van Serooskerke, X Schneider-Yin, R J Schimmel, et al.
American Journal of Human Genetics
|
January 1, 1995
Spectrum of mutations in the gene encoding the adrenoleukodystrophy protein
M J Ligtenberg, S Kemp, C O Sarde, et al.
Clinical Lung Cancer
|
June 19, 2025
Osimertinib Dose Optimization Guided by Therapeutic Drug Monitoring in Patients With EGFR-Mutated Advanced Non-Small Cell Lung Cancer: A Case series
Paul D Kruithof, Anita J W M Brouns, Juliette H R J Degens, et al.
European Respiratory Review : an Official Journal of the European Respiratory Society
|
June 15, 2022
Practical recommendations to combine small-molecule inhibitors and direct oral anticoagulants in patients with nonsmall cell lung cancer
Leila S Otten, Berber Piet, Michel M van den Heuvel, et al.
Maturitas
|
September 7, 2014
Increased fracture risk in patients with type 2 diabetes mellitus: an overview of the underlying mechanisms and the usefulness of imaging modalities and fracture risk assessment tools
Ellis A C de Waard, Tineke A C M van Geel, Hans H C M Savelberg, et al.
Platelets
|
June 24, 2006
Lorenzo's oil and platelet activation in adrenomyeloneuropathy and asymptomatic X-linked adrenoleukodystrophy
A Konijnenberg, B M van Geel, A Sturk, et al.
Biochemical and Biophysical Research Communications
|
July 29, 1994
Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutations
S Kemp, M J Ligtenberg, B M van Geel, et al.
Journal of the Peripheral Nervous System : JPNS
|
December 20, 2011
X-linked adrenomyeloneuropathy due to a novel missense mutation in the ABCD1 start codon presenting as demyelinating neuropathy
Marc Engelen, Anneke J van der Kooi, Stephan Kemp, et al.
Page
of 18