Search research articles
Contact Us
Filters
Showing results (11-20 of 38) with videos related to
Page
of 4
Sort By:
Cognitive and Behavioral Neurology : Official Journal of the Society for Behavioral and Cognitive Neurology
|
December 19, 2018
Alternating Hemiplegia of Childhood in Two Adult Patients with a Mild Syndrome
Katarzyna Ewa Polanowska, Karolina Dzieżyc, Hendrik Rosewich, et al.
BMC Medical Genetics
|
August 18, 2011
Characterization of two common 5' polymorphisms in PEX1 and correlation to survival in PEX1 peroxisome biogenesis disorder patients
Sven Thoms, Sabine Grønborg, Jana Rabenau, et al.
Infection
|
May 12, 2026
Disseminated cystic echinococcosis presenting as orbital swelling in a child - case report and literature review
Jonathan Remppis, Mariya Gosheva, Robert Rottscholl, et al.
Paediatric Anaesthesia
|
May 17, 2024
Factors Influencing Willingness to Participate in Clinical Studies in Pediatric Anesthesia (FILIPPA): A vignette-based, structured interview study
Clemens Miller, Jan Scholand, Johannes Wieditz, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 7, 2021
Clinical presentation and basic defect of the CFTR genotype p.Phe508del / p.Arg117His in a mother and her monozygous twin daughters
Christiane Lex, Rebecca Minso, Nadine Alfeis, et al.
Metabolites
|
June 2, 2021
LC-MS Based Platform Simplifies Access to Metabolomics for Peroxisomal Disorders
Henry Gerd Klemp, Matthias Kettwig, Frank Streit, et al.
Journal of Inherited Metabolic Disease
|
April 15, 2021
Targeted metabolomics revealed changes in phospholipids during the development of neuroinflammation in Abcd1<sup>tm1Kds</sup> mice and X-linked adrenoleukodystrophy patients
Matthias Kettwig, Henry Klemp, Stefan Nessler, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 25, 2015
Absence of biochemical evidence at an early age delays diagnosis in a patient with a clinically severe peroxisomal biogenesis disorder
Natalia Lüsebrink, Luciana Porto, Hans R Waterham, et al.
European Journal of Pediatrics
|
February 24, 2005
Colorectal cancer in two pre-teenage siblings with familial adenomatous polyposis
Silvija Jerkic, Hendrik Rosewich, Jens-Gerd Scharf, et al.
Neuropediatrics
|
January 17, 2022
How to Detect Isolated PEX10-Related Cerebellar Ataxia?
Esmeralda Nava, Britta Hartmann, Larissa Boxheimer, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 38) with videos related to
Sort By:
Page
of 4
Cognitive and Behavioral Neurology : Official Journal of the Society for Behavioral and Cognitive Neurology
|
December 19, 2018
Alternating Hemiplegia of Childhood in Two Adult Patients with a Mild Syndrome
Katarzyna Ewa Polanowska, Karolina Dzieżyc, Hendrik Rosewich, et al.
BMC Medical Genetics
|
August 18, 2011
Characterization of two common 5' polymorphisms in PEX1 and correlation to survival in PEX1 peroxisome biogenesis disorder patients
Sven Thoms, Sabine Grønborg, Jana Rabenau, et al.
Infection
|
May 12, 2026
Disseminated cystic echinococcosis presenting as orbital swelling in a child - case report and literature review
Jonathan Remppis, Mariya Gosheva, Robert Rottscholl, et al.
Paediatric Anaesthesia
|
May 17, 2024
Factors Influencing Willingness to Participate in Clinical Studies in Pediatric Anesthesia (FILIPPA): A vignette-based, structured interview study
Clemens Miller, Jan Scholand, Johannes Wieditz, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 7, 2021
Clinical presentation and basic defect of the CFTR genotype p.Phe508del / p.Arg117His in a mother and her monozygous twin daughters
Christiane Lex, Rebecca Minso, Nadine Alfeis, et al.
Metabolites
|
June 2, 2021
LC-MS Based Platform Simplifies Access to Metabolomics for Peroxisomal Disorders
Henry Gerd Klemp, Matthias Kettwig, Frank Streit, et al.
Journal of Inherited Metabolic Disease
|
April 15, 2021
Targeted metabolomics revealed changes in phospholipids during the development of neuroinflammation in Abcd1<sup>tm1Kds</sup> mice and X-linked adrenoleukodystrophy patients
Matthias Kettwig, Henry Klemp, Stefan Nessler, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 25, 2015
Absence of biochemical evidence at an early age delays diagnosis in a patient with a clinically severe peroxisomal biogenesis disorder
Natalia Lüsebrink, Luciana Porto, Hans R Waterham, et al.
European Journal of Pediatrics
|
February 24, 2005
Colorectal cancer in two pre-teenage siblings with familial adenomatous polyposis
Silvija Jerkic, Hendrik Rosewich, Jens-Gerd Scharf, et al.
Neuropediatrics
|
January 17, 2022
How to Detect Isolated PEX10-Related Cerebellar Ataxia?
Esmeralda Nava, Britta Hartmann, Larissa Boxheimer, et al.
Page
of 4