Detalhe da pesquisa
1.
Experience with tocilizumab in patients with neuromyelitis optica spectrum disorders.
Neurologia (Engl Ed)
; 37(3): 178-183, 2022 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-35465911
2.
Consensus statement on the use of alemtuzumab in daily clinical practice in Spain.
Neurologia (Engl Ed)
; 37(8): 615-630, 2022 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-36195374
3.
Consensus statement on the use of alemtuzumab in daily clinical practice in Spain. / Consenso de expertos sobre el uso de alemtuzumab en la práctica clínica diaria en España.
Neurologia (Engl Ed)
; 37(8): 615-630, 2022 10.
Artigo
Inglês, Espanhol
| MEDLINE | ID: mdl-31987648
4.
Experience with tocilizumab in patients with neuromyelitis optica spectrum disorders. / Experiencia con tocilizumab en pacientes con espectro de la neuromielitis óptica.
Neurologia (Engl Ed)
; 2019 Mar 27.
Artigo
Inglês, Espanhol
| MEDLINE | ID: mdl-30928236
5.
Development and validation of a brief electronic screening test for cognitive impairment in multiple sclerosis (SCI-MS Test).
Mult Scler Relat Disord
; 28: 50-56, 2019 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-30553169
6.
[Bucco-facial apraxia and anarthria, an exceptional debut form of corticobasal degeneration]. / Apraxia buco-facial y anartria, forma de comienzo excepcional de degeneración córticobasal.
An Med Interna
; 18(1): 50-1, 2001 Jan.
Artigo
Espanhol
| MEDLINE | ID: mdl-11387853
7.
Apraxia buco-facial y anartria, forma de comienzo excepcional de degeneración córticobasal / Anarthria, and buccofacial apraxia. A exceptional onset of corticobasal degeneration
An. med. interna (Madr., 1983)
; 18(1): 50-51, ene. 2001.
Artigo
Es
| IBECS (Espanha) | ID: ibc-8711
8.
[Clinical study of 8 families with various members affected with myotonic dystrophy of Curschmann Steinert's type]. / Estudio clínico de 8 familias con distintos miembros afectados de distrofia miotónica tipo Curschmann-Steinert.
Rev Clin Esp
; 157(5): 313-8, 1980 Jul 15.
Artigo
Espanhol
| MEDLINE | ID: mdl-7403605
9.
[Clinical study of 8 families with various members affected with myotonic dystrophy of Curshmann Steinert's type. Genetic considerations]. / Hallazgos complementarios en ocho familias afectas de distrofia miotónica Curschmann-Steinert. Consideraciones genéticas.
Rev Clin Esp
; 157(5): 319-23, 1980 Jul 15.
Artigo
Espanhol
| MEDLINE | ID: mdl-7403606