Mitochondrial membrane protein-associated neurodegeneration
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
- Mitochondrial membrane protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Rare ataxia
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Hereditary spastic paraplegia
- Huntington disease
- Leukodystrophy
- Classic pantothenate kinase-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Neuroferritinopathy
- Mitochondrial disease
- Atypical pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
Zentrum für mitochondriale Erkrankungen am LMU Klinikum München
Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum LMU Klinikum München
Ziemssenstraße 1
80336 München
089 440057400
089 440057402
Website
Email
- Leber hereditary optic neuropathy
- Recessive mitochondrial ataxia syndrome
- Pearson syndrome
- Mitochondrial neurogastrointestinal encephalomyopathy
- MELAS
- Kearns-Sayre syndrome
- Maternally-inherited diabetes and deafness
- Coenzyme Q10 deficiency
- MERRF
- Barth syndrome
- Mitochondrial myopathy
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Mitochondrial DNA depletion syndrome
- Mitochondrial membrane protein-associated neurodegeneration
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
- COASY protein-associated neurodegeneration
- Beta-propeller protein-associated neurodegeneration
- PLA2G6-associated neurodegeneration
- Adult-onset dystonia-parkinsonism
- Woodhouse-Sakati syndrome
- Pantothenate kinase-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Autosomal recessive spastic paraplegia type 35
- Fatty acid hydroxylase-associated neurodegeneration
- Kufor-Rakeb syndrome
- Infantile neuroaxonal dystrophy
- Aceruloplasminemia
- Neuroferritinopathy
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
- Mitochondrial membrane protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Rare ataxia
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Hereditary spastic paraplegia
- Huntington disease
- Leukodystrophy
- Classic pantothenate kinase-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Neuroferritinopathy
- Mitochondrial disease
- Atypical pantothenate kinase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
Zentrum für mitochondriale Erkrankungen am LMU Klinikum München
Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum LMU Klinikum München
Ziemssenstraße 1
80336 München
089 440057400
089 440057402
Website
Email
- Leber hereditary optic neuropathy
- Recessive mitochondrial ataxia syndrome
- Pearson syndrome
- Mitochondrial neurogastrointestinal encephalomyopathy
- MELAS
- Kearns-Sayre syndrome
- Maternally-inherited diabetes and deafness
- Coenzyme Q10 deficiency
- MERRF
- Barth syndrome
- Mitochondrial myopathy
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Mitochondrial DNA depletion syndrome
- Mitochondrial membrane protein-associated neurodegeneration
Supportgroups 1
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- COASY protein-associated neurodegeneration
- Beta-propeller protein-associated neurodegeneration
- PLA2G6-associated neurodegeneration
- Adult-onset dystonia-parkinsonism
- Woodhouse-Sakati syndrome
- Pantothenate kinase-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Autosomal recessive spastic paraplegia type 35
- Fatty acid hydroxylase-associated neurodegeneration
- Kufor-Rakeb syndrome
- Infantile neuroaxonal dystrophy
- Aceruloplasminemia
- Neuroferritinopathy