Neurodégénérescence associée à la protéine de membrane mitochondriale
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
- Diabète-surdité de transmission maternelle
- Déficit en coenzyme Q10
- Neurodégénérescence associée à la protéine de membrane mitochondriale
- Syndrome de Pearson
- Syndrome d'ataxie mitochondriale récessive
- Myopathie mitochondriale
- MERRF
- Syndrome de Barth
- Syndrome d'ataxie neuropathique sensorielle-dysarthrie-ophtalmoplégie
- Encéphalopathie myo-neuro-gastrointestinale
- MELAS
- Syndrome de déplétion de l'ADN mitochondrial
- Syndrome de Kearns-Sayre
- Neuropathie optique héréditaire de Leber
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
Website
Email
- Infantile neuroaxonal dystrophy
- Rare ataxia
- Mitochondrial membrane protein-associated neurodegeneration
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Hereditary spastic paraplegia
- Leukodystrophy
- Classic pantothenate kinase-associated neurodegeneration
- Myasthenia gravis
- Neurodegeneration with brain iron accumulation
- Neuroferritinopathy
- Atypical pantothenate kinase-associated neurodegeneration
- Mitochondrial disease
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
- PLA2G6-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Adult-onset dystonia-parkinsonism
- Pantothenate kinase-associated neurodegeneration
- Woodhouse-Sakati syndrome
- Neurodegeneration with brain iron accumulation
- Aceruloplasminemia
- Autosomal recessive spastic paraplegia type 35
- Fatty acid hydroxylase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Kufor-Rakeb syndrome
- 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
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
- Diabète-surdité de transmission maternelle
- Déficit en coenzyme Q10
- Neurodégénérescence associée à la protéine de membrane mitochondriale
- Syndrome de Pearson
- Syndrome d'ataxie mitochondriale récessive
- Myopathie mitochondriale
- MERRF
- Syndrome de Barth
- Syndrome d'ataxie neuropathique sensorielle-dysarthrie-ophtalmoplégie
- Encéphalopathie myo-neuro-gastrointestinale
- MELAS
- Syndrome de déplétion de l'ADN mitochondrial
- Syndrome de Kearns-Sayre
- Neuropathie optique héréditaire de Leber
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
Ziemssenstr. 1a
80336 München
089 440057400
089 440057402
Website
Email
- Infantile neuroaxonal dystrophy
- Rare ataxia
- Mitochondrial membrane protein-associated neurodegeneration
- Beta-propeller protein-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Huntington disease
- Hereditary spastic paraplegia
- Leukodystrophy
- Classic pantothenate kinase-associated neurodegeneration
- Myasthenia gravis
- Neurodegeneration with brain iron accumulation
- Neuroferritinopathy
- Atypical pantothenate kinase-associated neurodegeneration
- Mitochondrial disease
Supportgroups 1
Hoffnungsbaum e.V.
Wilhelm-Gülpen-Str. 22
52146
Würselen
- Beta-propeller protein-associated neurodegeneration
- PLA2G6-associated neurodegeneration
- COASY protein-associated neurodegeneration
- Adult-onset dystonia-parkinsonism
- Pantothenate kinase-associated neurodegeneration
- Woodhouse-Sakati syndrome
- Neurodegeneration with brain iron accumulation
- Aceruloplasminemia
- Autosomal recessive spastic paraplegia type 35
- Fatty acid hydroxylase-associated neurodegeneration
- Infantile neuroaxonal dystrophy
- Kufor-Rakeb syndrome
- Neuroferritinopathy