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Results of search for 'au:"Rallo, E"'
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Also-Rallo, E
Alías, L
Baiget, M
Barceló, M J
Beaumanoir, A
Bernal, S
Borrego, S
Fuentes-Prior, P
Guillén-Navarro, E
Gámez, J
Hernando, I
Hernández-Chico, C
Infante, F
Klein, D
Kraus-Ruppert, R
Martin, F
Martínez-Hernández, R
Millán, J M
Rallo, E
Tizzano, E F
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Adolescent
Adult
Aged
Biopsy
Child
Child, Preschool
Chondroitin
Chromatography, Ion Exchange
Electroencephalography
Epilepsy
Female
Glycosaminoglycans
Humans
Male
Muscular Atrophy, Spinal
Mutation
Pedigree
diagnosis
genetics
urine
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French
Your search returned 5 results.
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1.
[Familial progressive myoclonic epilepsy (Unverricht-Lundborg syndrome in five Valaisian families). A contribution to the research of its metabolic origin through the study of urinary excretion of mucopolysaccharides].
[electronic resource]
by
Rallo, E
Producer:
19710202
In:
Acta geneticae medicae et gemellologiae
vol. 18
Online resources:
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2.
[A large family of Valais affected with progressive myoclonic epilepsy and retinitis pigmentosa. A clinical, genetical and anatomo-pathological study].
[electronic resource]
by
Klein, D
Mumenthaler, M
Kraus-Ruppert, R
Rallo, E
Producer:
19690326
In:
Humangenetik
vol. 6
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3.
[Progressive malignant myoclonic epilepsy (Lafora's disease). Clinical and biochemical study of a case].
[electronic resource]
by
Rallo, E
Martin, F
Infante, F
Beaumanoir, A
Klein, D
Producer:
19690409
In:
Acta neurologica et psychiatrica Belgica
vol. 68
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4.
Improving detection and genetic counseling in carriers of spinal muscular atrophy with two copies of the SMN1 gene.
[electronic resource]
by
Alías, L
Barceló, M J
Bernal, S
Martínez-Hernández, R
Also-Rallo, E
Vázquez, C
Santana, A
Millán, J M
Baiget, M
Tizzano, E F
Producer:
20141121
In:
Clinical genetics
vol. 85
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5.
The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor.
[electronic resource]
by
Bernal, S
Alías, L
Barceló, M J
Also-Rallo, E
Martínez-Hernández, R
Gámez, J
Guillén-Navarro, E
Rosell, J
Hernando, I
Rodríguez-Alvarez, F J
Borrego, S
Millán, J M
Hernández-Chico, C
Baiget, M
Fuentes-Prior, P
Tizzano, E F
Producer:
20101215
In:
Journal of medical genetics
vol. 47
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