Literature DB >> 2043794

Pituitary growth hormone and Creutzfeldt-Jakob disease.

M E Macario, M Vaisman, A Buescu, V Moura Neto, H M Araujo, C Chagas.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 2043794      PMCID: PMC1669802          DOI: 10.1136/bmj.302.6785.1149

Source DB:  PubMed          Journal:  BMJ        ISSN: 0959-8138


× No keyword cloud information.
  5 in total

1.  Mortality, neoplasia, and Creutzfeldt-Jakob disease in patients treated with human pituitary growth hormone in the United Kingdom.

Authors:  C R Buchanan; M A Preece; R D Milner
Journal:  BMJ       Date:  1991-04-06

2.  Abnormal proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease.

Authors:  M G Harrington; C R Merril; D M Asher; D C Gajdusek
Journal:  N Engl J Med       Date:  1986-07-31       Impact factor: 91.245

3.  Creutzfeldt-Jakob disease following pituitary-derived human growth hormone therapy: a new American case.

Authors:  D J Marzewski; J Towfighi; M G Harrington; C R Merril; P Brown
Journal:  Neurology       Date:  1988-07       Impact factor: 9.910

4.  A new case of Creutzfeldt-Jakob disease associated with human growth hormone therapy in New Zealand.

Authors:  M Croxson; P Brown; B Synek; M G Harrington; R Frith; G Clover; J Wilson; D C Gajdusek
Journal:  Neurology       Date:  1988-07       Impact factor: 9.910

5.  Microheterogeneity of tubulin proteins in neuronal and glial cells from the mouse brain in culture.

Authors:  V Moura Neto; M Mallat; C Jeantet; A Prochiantz
Journal:  EMBO J       Date:  1983       Impact factor: 11.598

  5 in total
  3 in total

Review 1.  Etiology and pathogenesis of prion diseases.

Authors:  S J DeArmond; S B Prusiner
Journal:  Am J Pathol       Date:  1995-04       Impact factor: 4.307

2.  A further British case of growth hormone induced Creutzfeldt-Jakob disease.

Authors:  C J Ellis; H Katifi; R O Weller
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-12       Impact factor: 10.154

3.  Creutzfeldt-Jakob disease associated with a missense mutation at codon 200 of the prion protein gene in Brazil.

Authors:  Jerusa Smid; Vilma Regina Martins; Michele Christine Landemberger; Daniele Riva; Renato Anghinah; Ricardo Nitrini
Journal:  Dement Neuropsychol       Date:  2007 Apr-Jun
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.