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International Journal of Neonatal Screening
|
February 4, 2021
Gunnar Jungner and the Principles and Practice of Screening for Disease
Lars Jungner, Ingmar Jungner, Martin Engvall, et al.
Lakartidningen
|
March 11, 2020
[Ataxia - a group of heterogeneous diseases]
Martin Paucar, Niklas Dahl, Martin Engvall, et al.
Neurology. Genetics
|
June 19, 2023
Systemic Capillary Leak Syndrome With Cerebral Involvement in a <i>C9orf72</i> Expansion Carrier: Case Report and Review of the Literature
Stefan Sennfält, Oskar Aspegren, Martin Engvall, et al.
Cerebellum (London, England)
|
April 14, 2016
POLG-Associated Ataxia Presenting as a Fragile X Tremor/Ataxia Phenocopy Syndrome
Martin Paucar, Martin Engvall, Lisa Gordon, et al.
Investigative Ophthalmology & Visual Science
|
October 4, 2024
Ganglion Cell Complex Thickness and Visual Function in Chronic Leber Hereditary Optic Neuropathy
Johan Hedström, Maria Nilsson, Martin Engvall, et al.
Frontiers in Ophthalmology
|
June 30, 2026
Health-related quality of life and tobacco and alcohol consumption in Leber hereditary optic neuropathy in Sweden
Johan Hedström, Maria Nilsson, Martin Engvall, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 26, 2024
Comment to: "SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies"
Martin Paucar, Daniel Nilsson, Martin Engvall, et al.
Upsala Journal of Medical Sciences
|
January 18, 2012
Substrate reduction therapy with miglustat for type 1 Gaucher disease: a retrospective analysis from a single institution
Maciej Machaczka, Robert Hast, Ingrid Dahlman, et al.
Analytical Biochemistry
|
October 31, 2025
Advancing a sensitive method for measuring mitochondrial ATP production in small muscle biopsy samples
Rolf Wibom, David Alsina, Karin Naess, et al.
Journal of Neuromuscular Diseases
|
November 19, 2016
Epidemiology and Screening for Pompe Disease in Sweden
Hasan Balcin, Christopher Lindberg, Björn Lindvall, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 44) with videos related to
Sort By:
Page
of 5
International Journal of Neonatal Screening
|
February 4, 2021
Gunnar Jungner and the Principles and Practice of Screening for Disease
Lars Jungner, Ingmar Jungner, Martin Engvall, et al.
Lakartidningen
|
March 11, 2020
[Ataxia - a group of heterogeneous diseases]
Martin Paucar, Niklas Dahl, Martin Engvall, et al.
Neurology. Genetics
|
June 19, 2023
Systemic Capillary Leak Syndrome With Cerebral Involvement in a <i>C9orf72</i> Expansion Carrier: Case Report and Review of the Literature
Stefan Sennfält, Oskar Aspegren, Martin Engvall, et al.
Cerebellum (London, England)
|
April 14, 2016
POLG-Associated Ataxia Presenting as a Fragile X Tremor/Ataxia Phenocopy Syndrome
Martin Paucar, Martin Engvall, Lisa Gordon, et al.
Investigative Ophthalmology & Visual Science
|
October 4, 2024
Ganglion Cell Complex Thickness and Visual Function in Chronic Leber Hereditary Optic Neuropathy
Johan Hedström, Maria Nilsson, Martin Engvall, et al.
Frontiers in Ophthalmology
|
June 30, 2026
Health-related quality of life and tobacco and alcohol consumption in Leber hereditary optic neuropathy in Sweden
Johan Hedström, Maria Nilsson, Martin Engvall, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 26, 2024
Comment to: "SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies"
Martin Paucar, Daniel Nilsson, Martin Engvall, et al.
Upsala Journal of Medical Sciences
|
January 18, 2012
Substrate reduction therapy with miglustat for type 1 Gaucher disease: a retrospective analysis from a single institution
Maciej Machaczka, Robert Hast, Ingrid Dahlman, et al.
Analytical Biochemistry
|
October 31, 2025
Advancing a sensitive method for measuring mitochondrial ATP production in small muscle biopsy samples
Rolf Wibom, David Alsina, Karin Naess, et al.
Journal of Neuromuscular Diseases
|
November 19, 2016
Epidemiology and Screening for Pompe Disease in Sweden
Hasan Balcin, Christopher Lindberg, Björn Lindvall, et al.
Page
of 5