Search research articles
Contact Us
Filters
Showing results (41-50 of 58) with videos related to
Page
of 6
Sort By:
Journal of Alzheimer'S Disease : JAD
|
June 10, 2011
APOE and AβPP gene variation in cortical and cerebrovascular amyloid-β pathology and Alzheimer's disease: a population-based analysis
Terhi Peuralinna, Maarit Tanskanen, Mira Mäkelä, et al.
Nature Neuroscience
|
March 14, 2025
Sympathetic and parasympathetic subtypes of body-first Lewy body disease observed in postmortem tissue from prediagnostic individuals
Katrine B Andersen, Anushree Krishnamurthy, Mie Kristine Just, et al.
American Journal of Medical Genetics
|
March 29, 2002
ApoE epsilon3-haplotype modulates Alzheimer beta-amyloid deposition in the brain
Liisa Myllykangas, Tuomo Polvikoski, Karoliina Reunanen, et al.
Neuromuscular Disorders : NMD
|
December 22, 2024
Desmoid tumour: a rare cause of congenital unilateral calf enlargement mimicking calf hypertrophy
Maha Elseed, James N Sampson, Tuomo Polvikoski, et al.
Neuromuscular Disorders : NMD
|
June 19, 2017
Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domains
Elizabeth Harris, Umar Burki, Chiara Marini-Bettolo, et al.
Brain : a Journal of Neurology
|
June 28, 2024
Limbic-predominant age-related TDP-43 encephalopathy in the oldest old: a population-based study
Elizaveta Mikhailenko, Kia Colangelo, Jarno Tuimala, et al.
Sleep
|
July 9, 2018
Melatonin receptor type 1A gene linked to Alzheimer's disease in old age
Sonja Sulkava, Pranuthi Muggalla, Raimo Sulkava, et al.
Annals of Clinical and Translational Neurology
|
September 25, 2015
Genome-wide association study of neocortical Lewy-related pathology
Terhi Peuralinna, Liisa Myllykangas, Minna Oinas, et al.
Brain : a Journal of Neurology
|
December 28, 2010
A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophy
Debbie Hicks, Anna Sarkozy, Nuria Muelas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 9, 2018
Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease
Veronika Boczonadi, Martin S King, Anthony C Smith, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 58) with videos related to
Sort By:
Page
of 6
Journal of Alzheimer'S Disease : JAD
|
June 10, 2011
APOE and AβPP gene variation in cortical and cerebrovascular amyloid-β pathology and Alzheimer's disease: a population-based analysis
Terhi Peuralinna, Maarit Tanskanen, Mira Mäkelä, et al.
Nature Neuroscience
|
March 14, 2025
Sympathetic and parasympathetic subtypes of body-first Lewy body disease observed in postmortem tissue from prediagnostic individuals
Katrine B Andersen, Anushree Krishnamurthy, Mie Kristine Just, et al.
American Journal of Medical Genetics
|
March 29, 2002
ApoE epsilon3-haplotype modulates Alzheimer beta-amyloid deposition in the brain
Liisa Myllykangas, Tuomo Polvikoski, Karoliina Reunanen, et al.
Neuromuscular Disorders : NMD
|
December 22, 2024
Desmoid tumour: a rare cause of congenital unilateral calf enlargement mimicking calf hypertrophy
Maha Elseed, James N Sampson, Tuomo Polvikoski, et al.
Neuromuscular Disorders : NMD
|
June 19, 2017
Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domains
Elizabeth Harris, Umar Burki, Chiara Marini-Bettolo, et al.
Brain : a Journal of Neurology
|
June 28, 2024
Limbic-predominant age-related TDP-43 encephalopathy in the oldest old: a population-based study
Elizaveta Mikhailenko, Kia Colangelo, Jarno Tuimala, et al.
Sleep
|
July 9, 2018
Melatonin receptor type 1A gene linked to Alzheimer's disease in old age
Sonja Sulkava, Pranuthi Muggalla, Raimo Sulkava, et al.
Annals of Clinical and Translational Neurology
|
September 25, 2015
Genome-wide association study of neocortical Lewy-related pathology
Terhi Peuralinna, Liisa Myllykangas, Minna Oinas, et al.
Brain : a Journal of Neurology
|
December 28, 2010
A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophy
Debbie Hicks, Anna Sarkozy, Nuria Muelas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 9, 2018
Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease
Veronika Boczonadi, Martin S King, Anthony C Smith, et al.
Page
of 6