Publicacions científiques

Guinot-Bachero J, Balaguer-López E, Loma-Osorio Alonso del Real R, Rivera-Álvarez A, Ros-Mora MC, González-Jiménez F, Garralón-Pérez A, Herrera-Herzog E, Gombau-Baldrich Y, García-Molina P.

Any publicació:

2018

Número de revista:

Revista ROL de Enfermería vol. 41 n. 2

http://www.e-rol.es/sumari/sumari.php

Article

Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48).

Autor/s:

Genis D, Ortega-Cubero S, San Nicolás H, Corral J, Gardenyes J, de Jorge L, López E, Campos B, Lorenzo E, Tonda R, Beltran S, Negre M, Obón M, Beltran B, Fàbregas L, Alemany B, Márquez F, Ramió-Torrentà L, Gich J, Volpini V, Pastor P.

Any publicació:

2018

Número de revista:

Neurology vol. 91 n. 21

http://n.neurology.org/content/91/21/e1988.abstract

Article

High plasma levels of ghrelin and des-acyl ghrelin in responders to antiepileptic drugs

Autor/s:

Marchiò M, Roli L, Giordano C, Caramaschi E, Guerra A, Trenti T, Biagini G.

Any publicació:

2018

Número de revista:

Neurology vol. 91 n. 1

http://n.neurology.org/content/91/1/e62.abstract

Cas clínic

High-altitude cerebral edema or acute demyelinating encephalomyelitis in the Himalayas.

Autor/s:

Hensel O, Niroula P, Paudel R, Sherpa T, Kraya T, Presek P, Zierz S

Any publicació:

2018

Número de revista:

Neurology® Clinical Practice vol. 8 n. 1

http://cp.neurology.org/content/8/1/77

Una iniciativa de:

Cercador

Hemispatial neglect following right hemisphere stroke: clinical course and sensitivity of diagnostic tasks.

Hemodynamic assessments of venous pulsatile tinnitus using 4D-flow MRI

Hemophagocytic lymphohistiocytosis in 2 patients with multiple sclerosis treated with alemtuzumab.

Hemorrhagic encephalitis associated with H3N2 influenza A viral pneumonia

Hereditary spastic paraplegia presenting as limb dystonia with a rare SPG7 mutation Schaefer SM, Szekely AM, Moeller JJ, Tinaz S

Herida avulsiva compleja en pierna.

Heridas en Consultas de Enfermería de Atención Primaria. ¿Qué lesión genera mayor carga de trabajo? .

Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48).

High plasma levels of ghrelin and des-acyl ghrelin in responders to antiepileptic drugs

High-altitude cerebral edema or acute demyelinating encephalomyelitis in the Himalayas.

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