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Nature Reviews. Endocrinology
|
October 28, 2015
Dyslipidaemia: Lysosomal acid lipase deficiency-a cautious leap forward
Carla E M Hollak, G Kees Hovingh
Best Practice & Research. Clinical Endocrinology & Metabolism
|
May 20, 2015
The attenuated/late onset lysosomal storage disorders: Therapeutic goals and indications for enzyme replacement treatment in Gaucher and Fabry disease
Carla E M Hollak, Neal J Weinreb
Best Practice & Research. Clinical Endocrinology & Metabolism
|
May 20, 2015
The clinical spectrum and pathophysiology of skeletal complications in lysosomal storage disorders
Lorne A Clarke, Carla E M Hollak
Nederlands Tijdschrift Voor Geneeskunde
|
May 24, 2019
[Whole exome sequencing and whole genome sequencing in undiagnosed disease: of value for certain patient populations]
Gabor E Linthorst, Carla E M Hollak
Journal of Inherited Metabolic Disease
|
May 14, 2014
Treatment of lysosomal storage disorders: successes and challenges
Carla E M Hollak, Frits A Wijburg
Orphanet Journal of Rare Diseases
|
June 17, 2015
Quality of life in patients with Fabry disease: a systematic review of the literature
Maarten Arends, Carla E M Hollak, Marieke Biegstraaten
British Journal of Haematology
|
April 19, 2013
Malignancies and monoclonal gammopathy in Gaucher disease; a systematic review of the literature
Maarten Arends, Laura van Dussen, Marieke Biegstraaten, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
September 15, 2021
[The assessment of the price of a medicine: not only on the basis of the value for the patient]
Carla E M Hollak, Sibren van den Berg, Lonneke Timmers, et al.
Drug Discovery Today
|
February 19, 2018
Adaptive pathway development for Fabry disease: a clinical approach
Yvonne Schuller, Maarten Arends, Simon Körver, et al.
Current Pain and Headache Reports
|
September 3, 2013
Fabry disease: a rare cause of neuropathic pain
Marieke Biegstraaten, Gabor E Linthorst, Ivo N van Schaik, et al.
Page
of 20
Search research articles
Search
Showing results (1-10 of 194) with videos related to
Sort By:
Page
of 20
Nature Reviews. Endocrinology
|
October 28, 2015
Dyslipidaemia: Lysosomal acid lipase deficiency-a cautious leap forward
Carla E M Hollak, G Kees Hovingh
Best Practice & Research. Clinical Endocrinology & Metabolism
|
May 20, 2015
The attenuated/late onset lysosomal storage disorders: Therapeutic goals and indications for enzyme replacement treatment in Gaucher and Fabry disease
Carla E M Hollak, Neal J Weinreb
Best Practice & Research. Clinical Endocrinology & Metabolism
|
May 20, 2015
The clinical spectrum and pathophysiology of skeletal complications in lysosomal storage disorders
Lorne A Clarke, Carla E M Hollak
Nederlands Tijdschrift Voor Geneeskunde
|
May 24, 2019
[Whole exome sequencing and whole genome sequencing in undiagnosed disease: of value for certain patient populations]
Gabor E Linthorst, Carla E M Hollak
Journal of Inherited Metabolic Disease
|
May 14, 2014
Treatment of lysosomal storage disorders: successes and challenges
Carla E M Hollak, Frits A Wijburg
Orphanet Journal of Rare Diseases
|
June 17, 2015
Quality of life in patients with Fabry disease: a systematic review of the literature
Maarten Arends, Carla E M Hollak, Marieke Biegstraaten
British Journal of Haematology
|
April 19, 2013
Malignancies and monoclonal gammopathy in Gaucher disease; a systematic review of the literature
Maarten Arends, Laura van Dussen, Marieke Biegstraaten, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
September 15, 2021
[The assessment of the price of a medicine: not only on the basis of the value for the patient]
Carla E M Hollak, Sibren van den Berg, Lonneke Timmers, et al.
Drug Discovery Today
|
February 19, 2018
Adaptive pathway development for Fabry disease: a clinical approach
Yvonne Schuller, Maarten Arends, Simon Körver, et al.
Current Pain and Headache Reports
|
September 3, 2013
Fabry disease: a rare cause of neuropathic pain
Marieke Biegstraaten, Gabor E Linthorst, Ivo N van Schaik, et al.
Page
of 20