Suchergebnisse - "Cabral, Pedro"

PubPharm (71)

61

Rett syndrome with and without detected MECP2 mutations : an attempt to redefine phenotypes

enthalten in: Brain & development | 2011

von Temudo, T. | Santos, M. | Ramos, E. | +21

62

N170 asymmetry as an index of inferior occipital dysfunction in patients with symptomatic occipital lobe epilepsy

enthalten in: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology | 2011

von Lopes, R. | Cabral, P. | Canas, N. | +5

63

Rett syndrome with and without detected MECP2 mutations: An attempt to redefine phenotypes

enthalten in: Brain and development | 2011

von Temudo, T. | Santos, M. | Ramos, E. | +21

64

Needlescopic versus laparoscopic cholecystectomy. A prospective study of 60 patients

enthalten in: Acta cirurgica brasileira | 2008

von Cabral, P. | Silva, I. | Melo, J. | +3

65

Movement disorders in Rett syndrome : an analysis of 60 patients with detected MECP2 mutation and correlation with mutation type

enthalten in: Movement disorders : official journal of the Movement Disorder Society | 2008

von Temudo, T. | Ramos, E. | Dias, K. | +16

66

Long-term follow-up in Stuve-Wiedemann syndrome : a clinical report

enthalten in: American journal of medical genetics. Part A | 2008

von Gaspar, I. | Saldanha, T. | Cabral, P. | +6

67

Long-term follow-up in Stuve-Wiedemann syndrome: A clinical reportHow to cite this article: Gaspar IM, Saldanha T, Cabral P, Manuel Vilhena M, Tuna M, Costa C, Dagoneau N, Daire VC, Hennekam RCM. 2008. Long-term follow-up in Stuve-Wiedemann syndrome. Am J Med Genet Part A 146A:1748-1753.

enthalten in: American journal of medical genetics / C | 2008

von Gaspar, I. | Saldanha, T. | Cabral, P. | +6

68

Movement disorders in Rett syndrome: An analysis of 60 patients with detected MECP2 mutation and correlation with mutation type

enthalten in: Movement disorders | 2008

von Temudo, T. | Ramos, E. | Dias, K. | +16

69

Attention deficit disorders : are we barking up the wrong tree?

enthalten in: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society | 2006

von Cabral, P.

70

The mitochondrial DNA A3243G mutation in Portugal: clinical and molecular studies in 5 families

enthalten in: Journal of the neurological sciences | 1999

von Vilarinho, L. | Santorelli, F. | Coelho, I. | +8