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
- Leukodystrophy
- Hereditary spastic paraplegia
- Atypical pantothenate kinase-associated neurodegeneration
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial membrane protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Myasthenia gravis
- Beta-propeller protein-associated neurodegeneration
- Huntington disease
- Neuroferritinopathy
- Infantile neuroaxonal dystrophy
- Mitochondrial disease
- COASY protein-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Rare ataxia
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
- Maternally-inherited diabetes and deafness
- Mitochondrial neurogastrointestinal encephalomyopathy
- Mitochondrial membrane protein-associated neurodegeneration
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Barth syndrome
- Mitochondrial myopathy
- MERRF
- Leber hereditary optic neuropathy
- Recessive mitochondrial ataxia syndrome
- MELAS
- Mitochondrial DNA depletion syndrome
- Coenzyme Q10 deficiency
- Pearson syndrome
- Kearns-Sayre syndrome
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
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Neuroferritinopathy
- Adult-onset dystonia-parkinsonism
- PLA2G6-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Kufor-Rakeb syndrome
- Fatty acid hydroxylase-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Autosomal recessive spastic paraplegia type 35
- Aceruloplasminemia
- Woodhouse-Sakati syndrome
- Neurodegeneration with brain iron accumulation
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
Webseite
E-Mail
Care facilities 2
Friedrich-Baur-Institut der Neurologischen Klinik, am LMU Klinikum München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057470
089 440057402
Webseite
E-Mail
- Leukodystrophy
- Hereditary spastic paraplegia
- Atypical pantothenate kinase-associated neurodegeneration
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial membrane protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Myasthenia gravis
- Beta-propeller protein-associated neurodegeneration
- Huntington disease
- Neuroferritinopathy
- Infantile neuroaxonal dystrophy
- Mitochondrial disease
- COASY protein-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Rare ataxia
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
Webseite
E-Mail
- Maternally-inherited diabetes and deafness
- Mitochondrial neurogastrointestinal encephalomyopathy
- Mitochondrial membrane protein-associated neurodegeneration
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
- Barth syndrome
- Mitochondrial myopathy
- MERRF
- Leber hereditary optic neuropathy
- Recessive mitochondrial ataxia syndrome
- MELAS
- Mitochondrial DNA depletion syndrome
- Coenzyme Q10 deficiency
- Pearson syndrome
- Kearns-Sayre syndrome
Supportgroups 1
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Neuroferritinopathy
- Adult-onset dystonia-parkinsonism
- PLA2G6-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Kufor-Rakeb syndrome
- Fatty acid hydroxylase-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Autosomal recessive spastic paraplegia type 35
- Aceruloplasminemia
- Woodhouse-Sakati syndrome
- Neurodegeneration with brain iron accumulation