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Aran-Duchenne disease
Cruveilhier disease
Disease Charcot-Marie-Tooth
Distal
Déjerine-Sottas
Fazio-Londe
Infantile spinal muscular atrophy
Kugelberg-Welander
PMA
Primary
Progressive bulbar palsy
Progressive bulbar palsy of childhood
Progressive muscular atrophy
Progressive muscular atrophy of infancy
Progressive spinal muscular atrophy
SMA
SMA I
SPMA
Scapuloperoneal form
Severe infantile spinal muscular atrophy
Spinal muscular atrophy
Spinal muscular atrophy adult form
Spinal muscular atrophy type I
Spinal progressive muscular atrophy
Werdnig-Hoffman disease

Vertaling van "Progressive muscular atrophy infancy " (Engels → Nederlands) :

infantile spinal muscular atrophy | progressive muscular atrophy of infancy | severe infantile spinal muscular atrophy | spinal muscular atrophy type I | Werdnig-Hoffman disease | SMA I [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
infantiele spinale spieratrofie | Spinale musculaire atrofie type I | ziekte van Werdnig-Hoffmann | SMA type I [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Aran-Duchenne disease | Cruveilhier disease | PMA | progressive muscular atrophy | progressive spinal muscular atrophy | spinal muscular atrophy | spinal progressive muscular atrophy | SMA [Abbr.] | SPMA [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
spieratrofie van Aran-Duchenne | ziekte van Duchenne-Aran
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
A rare progressive muscular dystrophy characterized by an adult-onset scapulo-axio-peroneal myopathy. Clinical presentation includes shoulder girdle atrophy, scapular winging, axial muscular atrophy of postural muscles combined with a generalized hyp
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
X-gebonden myopathie met posturale spieratrofie
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Disease:Charcot-Marie-Tooth | Déjerine-Sottas | Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal type)(hypertrophic type) Roussy-Lévy syndrome
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
hereditaire motorische- en sensorische-neuropathie, type I-IV | infantiele hypertrofische-neuropathie | peroneale spieratrofie (axonaal type)(hypertrofisch type) | syndroom van Roussy-Lévy | ziekte van | Charcot-Marie-Tooth | ziekte van | Déjerine-Sottas
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
A rare non-dystrophic myopathy with characteristics of slowly progressive muscular weakness and atrophy initially involving proximal lower limbs and hip girdle and later on shoulder girdle, proximal upper limbs and axial muscles. Ambulation is usuall
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
HIBM4 - hereditary inclusion body myopathy type 4
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Familial motor neuron disease Lateral sclerosis:amyotrophic | primary | Progressive:bulbar palsy | spinal muscular atrophy
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
familiale ziekte van motorische neuronen | laterale sclerose | amyotrofe | laterale sclerose | primaire | progressieve | bulbairparalyse | progressieve | spinale spieratrofie
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
Progressive bulbar palsy of childhood [Fazio-Londe] Spinal muscular atrophy:adult form | childhood form, type II | distal | juvenile form, type III [Kugelberg-Welander] | scapuloperoneal form
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
progressieve bulbairparalyse in kinderjaren [Fazio-Londe] | spinale spieratrofie | distaal | spinale spieratrofie | juveniele vorm, type III [Kugelberg-Welander] | spinale spieratrofie | scapuloperoneale vorm | spinale spieratrofie | van kinderleeftijd, type II | spinale spieratrofie | volwassen vorm
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
A group of rare genetic neurodegenerative diseases with characteristics of infancy to childhood onset of progressive spastic paraplegia (with delayed motor milestones, gait disturbances, hyperreflexia and extensor plantar responses), optic atrophy (w
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
spastische paraplegie, opticusatrofie, neuropathie en aan spastische paraplegie, opticusatrofie en neuropathie-gerelateerde aandoening
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


Anderen hebben gezocht naar : aran-duchenne disease     cruveilhier disease     déjerine-sottas     fazio-londe     kugelberg-welander     progressive bulbar palsy of childhood     progressive bulbar palsy     spinal muscular atrophy adult form     werdnig-hoffman disease     childhood form type ii     distal     infantile spinal muscular atrophy     juvenile form type iii     primary     progressive muscular atrophy     progressive muscular atrophy of infancy     progressive spinal muscular atrophy     scapuloperoneal form     severe infantile spinal muscular atrophy     spinal muscular atrophy     spinal muscular atrophy type     spinal progressive muscular atrophy     Progressive muscular atrophy infancy     


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Date index: 2021-12-26
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