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 440057470
089 440057402
Website
Email
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Mitochondrial membrane protein-associated neurodegeneration
- Rare ataxia
- Hereditary spastic paraplegia
- Beta-propeller protein-associated neurodegeneration
- Leukodystrophy
- COASY protein-associated neurodegeneration
- Myasthenia gravis
- Neurodegeneration with brain iron accumulation
- Neuroferritinopathy
- Atypical pantothenate kinase-associated neurodegeneration
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial disease
- Infantile neuroaxonal dystrophy
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
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- MELAS
- Pearson syndrome
- MERRF
- Recessive mitochondrial ataxia syndrome
- Leber hereditary optic neuropathy
- Mitochondrial neurogastrointestinal encephalomyopathy
- Mitochondrial membrane protein-associated neurodegeneration
- Kearns-Sayre syndrome
- Coenzyme Q10 deficiency
- Barth syndrome
- Mitochondrial myopathy
- Maternally-inherited diabetes and deafness
Institut für Humangenetik am TUM Klinikum Rechts der Isar
TUM Klinikum Rechts der Isar
Trogerstr. 32
81675 München
089 41406381
089 41406382
Website
Email
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Aceruloplasminemia
- Autosomal recessive spastic paraplegia type 35
- Neurodegeneration with brain iron accumulation
- Infantile neuroaxonal dystrophy
- Kufor-Rakeb syndrome
- Woodhouse-Sakati syndrome
- PLA2G6-associated neurodegeneration
- Adult-onset dystonia-parkinsonism
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Neuroferritinopathy
- Fatty acid hydroxylase-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
Parent facilities 0
Genetic Advices 1
Institut für Humangenetik am TUM Klinikum Rechts der Isar
TUM Klinikum Rechts der Isar
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 440057470
089 440057402
Website
Email
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Mitochondrial membrane protein-associated neurodegeneration
- Rare ataxia
- Hereditary spastic paraplegia
- Beta-propeller protein-associated neurodegeneration
- Leukodystrophy
- COASY protein-associated neurodegeneration
- Myasthenia gravis
- Neurodegeneration with brain iron accumulation
- Neuroferritinopathy
- Atypical pantothenate kinase-associated neurodegeneration
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial disease
- Infantile neuroaxonal dystrophy
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
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- MELAS
- Pearson syndrome
- MERRF
- Recessive mitochondrial ataxia syndrome
- Leber hereditary optic neuropathy
- Mitochondrial neurogastrointestinal encephalomyopathy
- Mitochondrial membrane protein-associated neurodegeneration
- Kearns-Sayre syndrome
- Coenzyme Q10 deficiency
- Barth syndrome
- Mitochondrial myopathy
- Maternally-inherited diabetes and deafness
Supportgroups 1
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Aceruloplasminemia
- Autosomal recessive spastic paraplegia type 35
- Neurodegeneration with brain iron accumulation
- Infantile neuroaxonal dystrophy
- Kufor-Rakeb syndrome
- Woodhouse-Sakati syndrome
- PLA2G6-associated neurodegeneration
- Adult-onset dystonia-parkinsonism
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Neuroferritinopathy
- Fatty acid hydroxylase-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration