Search Results - "Cancho García, E" :: K.UTB vyhledávací portál

Mutation of the MMADHC gene in adult-onset cobalamin D deficiency: A report of 2 potentially treatable cases

by Cancho García, E, Geán, E, Oliver Tormo, B, Torrents, A, Esteban Durán, E
Published in Neurologia (Barcelona, Spain) (01.07.2019)

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Carotid agenesis and absence of bifurcation, asymptomatic and incidental, during the study of cognitive impairment: A case report

by Cancho García, E, Mora Monago, R
Published in Neurología (Barcelona, English ed. ) (19.12.2020)

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Carotid agenesis and absence of bifurcation, asymptomatic and incidental, during the study of cognitive impairment: a case report

by Cancho García, E., Mora Monago, R.
Published in Neurología (Barcelona, English ed. ) (01.11.2021)

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Mutación del gen MMADHC de la cobalamina D con comienzo en el adulto: a propósito de 2 casos potencialmente tratables

by Cancho García, E., Geán, E., Oliver Tormo, B., Torrents, A., Esteban Durán, E.
Published in Neurología (Barcelona, Spain) (01.07.2019)

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Agenesia carotídea y ausencia de bifurcación, asintomáticas e incidental, durante el estudio de deterioro cognitivo: a propósito de un caso

by Cancho García, E., Mora Monago, R.
Published in Neurología (Barcelona, Spain) (01.11.2021)

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Mutation of the MMADHC gene in adult-onset cobalamin D deficiency: a report of 2 potentially treatable cases

by Cancho García, E., Geán, E., Oliver Tormo, B., Torrents, A., Esteban Durán, E.
Published in Neurología (Barcelona, English ed. ) (01.07.2019)

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Carotid agenesis and absence of bifurcation, asymptomatic and incidental, during the study of cognitive impairment: a case report

by Cancho García, E, Mora Monago, R
Published in Neurologia (Barcelona, Spain) (01.11.2021)

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Cumplimiento de las guías de la Sociedad Española de Neurología en el tratamiento de los pacientes con esclerosis múltiple

by Oreja Guevara, Celia, Río Izquierdo, Jordi, Gobartt, Ana L., en nombre del grupo de investigador, en nombre del grupo de investigador
Published in Revista de neurologiá (01.08.2015)

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Cryoglobulinemia type II with double neuropathy not associated with hepatitis C infection

by Cancho-Garcia, E, Guillen-Sanchez, M V
Published in Revista de neurologiá (01.08.2016)

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Mutation of the MMADHC gene in adult-onset cobalamin D deficiency: A report of 2 potentially treatable cases

by Cancho García, E, Geán, E, Oliver Tormo, B, Torrents, A, Esteban Durán, E
Published in Neurologia (Barcelona, Spain) (01.07.2019)

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Cryoglobulinemia type II with double neuropathy not associated with hepatitis C infection

by Cancho-Garcia, E, Guillen-Sanchez, M V
Published in Revista de neurologia (01.08.2016)

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