«HEREDOATAXIA» தொடர்புடைய போர்ச்சுகீஸ் புத்தகங்கள்
பின்வரும் புத்தக விவரத்தொகுப்புத் தேர்ந்தெடுப்பில்
heredoataxia இன் பயன்பாட்டைக் கண்டறியுங்கள்.
heredoataxia தொடர்பான புத்தகங்கள் மற்றும் போர்ச்சுகீஸ் இலக்கியத்தில் அதன் பயன்பாட்டுச் சூழலை வழங்குவதற்கு அதிலிருந்து பெறப்பட்ட சுருக்கமான சாரங்களைத் தொடர்புபடுத்துகின்றன.
1
The Routledge Spanish Bilingual Dictionary of Psychology and ...
controversia (f) herencia-ambiente heredoataxia n — heredoataxia (f)
heredofamiiiai adj— heredofamiiiar heredofamiiiai psychosis — psicosis (f)
heredofamiiiar heredofamiiiai tremor — temblor (m) heredofamiiiar heredopathia
n ...
2
Visual System in Myelin Disorders
rial pathways, whereas the impairment of the nuclei is relatively rare except in
secondary demyelination with impairment of the neurons. These signs can be
very vague during initial period in heredoataxia and amyotrophic lateral sclerosis
or ...
A. Neetens, A. Lowenthal, J.J. Martin, 1984
3
The 5-minute Neurology Consult
Miscellaneous SYNONYMS Heredoataxia hemeralopica polyneuritiformis
Heredopathia atactica polyneuritiformis HMSN IV. ICD-9-CM: 356.3 Refsum's
disease SEE ALSO: PEROXISOMAL DISORDERS REFERENCES • Gibberd FB,
...
D. Joanne Lynn, Herbert B. Newton, Alexander Rae-Grant, 2004
4
Advances in Neurology: Proceedings of the Xivth World ...
Mollaret (1939) included cerebellar heredo-ataxia among the spinocerebellar
heredodegenerations, and Greenfield (1954) distinguished heredoataxia of the
Pierre-Marie type from the Menzel and Holmes types of cerebellar heredoataxia.
Jagjit S. Chopra, K. Jagannathan, I. M. S. Sawhney, 1990
5
Handbook of Clinical Neurology
... 443 Hereditary spinodentatonigro-oculomotor degeneration, 157-176
Hereditary tremor Roussy-Levy syndrome, 175 Hereditary ulceromutilating
acropathy, see Thevenard's disease Heredoataxia, 365 Africa, 36 als, 142 bulbar
paralysis, ...
P. J. Vinken, G. W. Bruyn, Harold L. Klawans, 1975
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Handbook of Neurochemistry: Experimental neurochemistry
... spastic metachromatic urine29; decrease of forms) diplegia28 substances
arylsulfatase A in leucocytes, fibroblasts. and cells of amniotic fluid30 Refsum
Heredoataxia and Heredoataxia and Increased phytanic acid polyneuritis.
increase of ...
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Pediatric neuropathology
Mollaret1 included cerebellar heredoataxia among the spinocerebellar
heredodegenerations, and Greenfield2 distinguished heredoataxia of the Marie
type from the Menzel and Holmes types. In fact, there is no satisfactory
classification of ...
8
Handbook of Clinical Neurology
... 13/ 178 274 strabismus, 13/274 Hereditary whispering dysphonia, see Focal
dystonia musculorum deformans Heredoataxia, see Hereditary cerebellar ataxia
Heredoataxia hemeralopica polyneuritiformis, see Refsum disease Heredoataxia
...
P. J. Vinken, G. W. Bruyn, 2002
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Proceedings of the ... International Congress of Human Genetics
cerebellar ataxia". I dislike the idea of changing it once more. If I had known when
I termed the syndrome what the neuropathologists now have told me, I would
have preferred to use the name heredoataxia polyneuritiformis. REFERENCES 1.
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Enciclopedia Salvat de ciencias me(dicas
Enfermsdad rara, familiar, caracterizada por ataques paroxismales de parálisis,
asociados con dolor intenso en las extremidades y sensación de debilidad.
HEREDOATAXIA. Ataxia familiar o enfermedad de Friedreich. II —
espinocerebelosa.
Jaime Valero-Ribas, Salvat Editores (Barcelona, Spain), 1959
இல் உள்ள வார்த்தைகளில் மறைக்கப்பட்டிருக்கும் எல்லாவற்றையும் கண்டறியுங்கள் 
