Literature DB >> 13007229

Progressive bulbar paralysis showing heredofamilial incidence and intellectual impairment.

E E ROBERTSON.   

Abstract

Entities:  

Keywords:  BULBAR PALSY/manifestations; MENTAL DISORDERS

Mesh：

Year:  1953        PMID： 13007229

Source DB:  PubMed          Journal:  AMA Arch Neurol Psychiatry        ISSN： 0096-6886


× No keyword cloud information.
  6 in total

1.  A genetic study of progressive spinal muscular atrophy.

Authors:  N C MYRIANTHOPOULOS; I A BROWN
Journal:  Am J Hum Genet       Date:  1954-12       Impact factor: 11.025

2.  [On the genetics and demography of Charcot's disease in the area of Westphalia].

Authors:  W F HABERLANDT
Journal:  Dtsch Z Nervenheilkd       Date:  1959

3.  Molecular evaluation of human ubiquilin 2 gene PXX domain in familial frontotemporal dementia patients.

Authors:  Isabel Hernández; Anna Espinosa; Luis Miguel Real; Jose Jorge Galán; Ana Mauleón; Maiteé Rosende Roca; Lluís Tárraga; Agustín Ruiz; Mercè Boada
Journal:  J Neurol       Date:  2012-06-24       Impact factor: 4.849

4.  [Genetic relations between myatrophies and psychoses].

Authors:  K H PARNITZKE; R SEIDEL
Journal:  Dtsch Z Nervenheilkd       Date:  1961

5.  Cerebral lesions in familial amyotrophic lateral sclerosis and dementia.

Authors:  M H Finlayson; J B Martin
Journal:  Acta Neuropathol       Date:  1973-11-05       Impact factor: 17.088

6.  Motor neuron disease and frontotemporal dementia: One, two, or three diseases?

Authors:  Thomas H Bak
Journal:  Ann Indian Acad Neurol       Date:  2010-12       Impact factor: 1.383
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.