Neurodégénérescence associée à la protéine de membrane mitochondriale
All Entries 4
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
Website
Email
- Neurodegeneration with brain iron accumulation
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial disease
- Myasthenia gravis
- Beta-propeller protein-associated neurodegeneration
- Leukodystrophy
- COASY protein-associated neurodegeneration
- Rare ataxia
- Mitochondrial membrane protein-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Pantothenate kinase-associated neurodegeneration
- Hereditary spastic paraplegia
- Huntington disease
- Atypical pantothenate kinase-associated neurodegeneration
- Neuroferritinopathy
Zentrum für mitochondriale Erkrankungen am LMU Klinikum München
Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum
Ziemssenstraße 1
80336 München
089 440057400
089 440057402
Website
Email
- Mitochondrial DNA depletion syndrome
- MELAS
- MERRF
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Barth syndrome
- Mitochondrial myopathy
- Kearns-Sayre syndrome
- Coenzyme Q10 deficiency
- Recessive mitochondrial ataxia syndrome
- Maternally-inherited diabetes and deafness
- Leber hereditary optic neuropathy
- Mitochondrial neurogastrointestinal encephalomyopathy
- Pearson syndrome
Institut für Humangenetik am Klinikums rechts der Isar der Technischen Universität München
Klinikum rechts der Isar der Technischen Universität München
Trogerstr. 32
81675 München
089 41406381
089 41406382
Website
Email
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Beta-propeller protein-associated neurodegeneration
- Neuroferritinopathy
- Adult-onset dystonia-parkinsonism
- PLA2G6-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Kufor-Rakeb syndrome
- COASY protein-associated neurodegeneration
- Woodhouse-Sakati syndrome
- Neurodegeneration with brain iron accumulation
- Aceruloplasminemia
- Autosomal recessive spastic paraplegia type 35
- Fatty acid hydroxylase-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
Parent facilities 0
Genetic Advices 1
Institut für Humangenetik am Klinikums rechts der Isar der Technischen Universität München
Klinikum rechts der Isar der Technischen Universität München
Trogerstr. 32
81675 München
089 41406381
089 41406382
Website
Email
Care facilities 2
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
Website
Email
- Neurodegeneration with brain iron accumulation
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial disease
- Myasthenia gravis
- Beta-propeller protein-associated neurodegeneration
- Leukodystrophy
- COASY protein-associated neurodegeneration
- Rare ataxia
- Mitochondrial membrane protein-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Pantothenate kinase-associated neurodegeneration
- Hereditary spastic paraplegia
- Huntington disease
- Atypical pantothenate kinase-associated neurodegeneration
- Neuroferritinopathy
Zentrum für mitochondriale Erkrankungen am LMU Klinikum München
Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum
Ziemssenstraße 1
80336 München
089 440057400
089 440057402
Website
Email
- Mitochondrial DNA depletion syndrome
- MELAS
- MERRF
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Mitochondrial membrane protein-associated neurodegeneration
- Barth syndrome
- Mitochondrial myopathy
- Kearns-Sayre syndrome
- Coenzyme Q10 deficiency
- Recessive mitochondrial ataxia syndrome
- Maternally-inherited diabetes and deafness
- Leber hereditary optic neuropathy
- Mitochondrial neurogastrointestinal encephalomyopathy
- Pearson syndrome
Supportgroups 1
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Beta-propeller protein-associated neurodegeneration
- Neuroferritinopathy
- Adult-onset dystonia-parkinsonism
- PLA2G6-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Kufor-Rakeb syndrome
- COASY protein-associated neurodegeneration
- Woodhouse-Sakati syndrome
- Neurodegeneration with brain iron accumulation
- Aceruloplasminemia
- Autosomal recessive spastic paraplegia type 35
- Fatty acid hydroxylase-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration