Mitochondrial membrane protein-associated neurodegeneration
All Entries 4
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
- Leber hereditary optic neuropathy
- Coenzyme Q10 deficiency
- Barth syndrome
- Mitochondrial myopathy
- MELAS
- Recessive mitochondrial ataxia syndrome
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Pearson syndrome
- Mitochondrial neurogastrointestinal encephalomyopathy
- MERRF
- Maternally-inherited diabetes and deafness
- Kearns-Sayre syndrome
- Mitochondrial DNA depletion syndrome
- Mitochondrial membrane protein-associated neurodegeneration
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057470
089 440057402
Website
Email
- Beta-propeller protein-associated neurodegeneration
- Neuroferritinopathy
- Mitochondrial disease
- COASY protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Infantile neuroaxonal dystrophy
- Classic pantothenate kinase-associated neurodegeneration
- Myasthenia gravis
- Atypical pantothenate kinase-associated neurodegeneration
- Mitochondrial membrane protein-associated neurodegeneration
- Leukodystrophy
- Hereditary spastic paraplegia
- Rare ataxia
- Neurodegeneration with brain iron accumulation
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
- Neurodegeneration with brain iron accumulation
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Autosomal recessive spastic paraplegia type 35
- Pantothenate kinase-associated neurodegeneration
- Woodhouse-Sakati syndrome
- Adult-onset dystonia-parkinsonism
- PLA2G6-associated neurodegeneration
- Fatty acid hydroxylase-associated neurodegeneration
- Kufor-Rakeb syndrome
- Infantile neuroaxonal dystrophy
- Neuroferritinopathy
- Aceruloplasminemia
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
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
- Leber hereditary optic neuropathy
- Coenzyme Q10 deficiency
- Barth syndrome
- Mitochondrial myopathy
- MELAS
- Recessive mitochondrial ataxia syndrome
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Pearson syndrome
- Mitochondrial neurogastrointestinal encephalomyopathy
- MERRF
- Maternally-inherited diabetes and deafness
- Kearns-Sayre syndrome
- Mitochondrial DNA depletion syndrome
- Mitochondrial membrane protein-associated neurodegeneration
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057470
089 440057402
Website
Email
- Beta-propeller protein-associated neurodegeneration
- Neuroferritinopathy
- Mitochondrial disease
- COASY protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Infantile neuroaxonal dystrophy
- Classic pantothenate kinase-associated neurodegeneration
- Myasthenia gravis
- Atypical pantothenate kinase-associated neurodegeneration
- Mitochondrial membrane protein-associated neurodegeneration
- Leukodystrophy
- Hereditary spastic paraplegia
- Rare ataxia
- Neurodegeneration with brain iron accumulation
Supportgroups 1
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Neurodegeneration with brain iron accumulation
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Autosomal recessive spastic paraplegia type 35
- Pantothenate kinase-associated neurodegeneration
- Woodhouse-Sakati syndrome
- Adult-onset dystonia-parkinsonism
- PLA2G6-associated neurodegeneration
- Fatty acid hydroxylase-associated neurodegeneration
- Kufor-Rakeb syndrome
- Infantile neuroaxonal dystrophy
- Neuroferritinopathy
- Aceruloplasminemia