Zobrazeno 1 - 7
of 7
pro vyhledávání: '"M L, Franz"'
Publikováno v:
The Journal of Neuropsychiatry and Clinical Neurosciences. 6:147-153
This study assessed the frequency and type of sexual disorders associated with Huntington's disease (HD) in an unbiased sample. Of 39 HD patients and 32 of their partners, 82% and 66%, respectively, had one or more sexual disorders by DSM-III-R crite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98f023f7f3a71dc12eb6e627b915fe4d
https://doi.org/10.1176/jnp.6.2.147
https://doi.org/10.1176/jnp.6.2.147
Autor:
A, Rosenblatt, R R, Brinkman, K Y, Liang, E W, Almqvist, R L, Margolis, C Y, Huang, M, Sherr, M L, Franz, M H, Abbott, M R, Hayden, C A, Ross
Publikováno v:
American journal of medical genetics. 105(5)
In order to provide data relevant to a search for modifying genes for age of onset in Huntington disease, we examined the relationship between CAG number and age of onset in a total of 370 individuals from 165 siblingships, in two cohorts of siblings
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2b3143b17de3d2a0de9fac75a194e251
https://pubmed.ncbi.nlm.nih.gov/11449389
https://pubmed.ncbi.nlm.nih.gov/11449389
Autor:
M. L. Franz, P. S. Harper, Jayne Leggo, Mark W. Becher, M. Sherr, M. H. Abbott, J. C. Macmillan, L. Barron, M. Porteous, David C. Rubinsztein, O. C. Stine, M. V. Wagster, Christopher A. Ross, N. G. Ranen
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 12(4)
Dentatorubral and pallidoluysian atrophy (DRPLA) is an autosomal dominant disorder that clinically overlaps with Huntington's disease (HD) and manifests combinations of chorea, myoclonus, seizures, ataxia, and dementia. DRPLA is caused by a CAG tripl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b07c55e9cba65279fa78458c38d599c
https://pubmed.ncbi.nlm.nih.gov/9756163
https://pubmed.ncbi.nlm.nih.gov/9756163
Autor:
N G, Ranen, O C, Stine, M H, Abbott, M, Sherr, A M, Codori, M L, Franz, N I, Chao, A S, Chung, N, Pleasant, C, Callahan
Publikováno v:
American journal of human genetics. 57(3)
Huntington disease (HD) is an autosomal dominant degenerative disorder caused by an expanded and unstable trinucleotide repeat (CAG)n in a gene (IT-15) on chromosome 4. HD exhibits genetic anticipation--earlier onset in successive generations within
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4788d46dfa50645449f574e8af4dff45
https://pubmed.ncbi.nlm.nih.gov/7668287
https://pubmed.ncbi.nlm.nih.gov/7668287
Publikováno v:
The American Journal of Clinical Nutrition. 30:512-516
The use of a simple, hypoallergenic elemental diet would appear well suited for diagnosing food allergy. Vivonex was used in 21 patients (5 to 40 years old) suspected of food allergy or those who had failed to respond to the usual management of inhal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9d025c93b890f3d5ace3e58ae07fd2b
https://doi.org/10.1093/ajcn/30.4.512
https://doi.org/10.1093/ajcn/30.4.512
Autor:
J, Brandt, K A, Quaid, S E, Folstein, P, Garber, N E, Maestri, M H, Abbott, P R, Slavney, M L, Franz, L, Kasch, H H, Kazazian
Publikováno v:
JAMA. 261(21)
Clinical medicine in the 21st century is almost certain to include wide-scale use of molecular genetic diagnostic tests. In September 1986, The Johns Hopkins University School of Medicine initiated a voluntary program of presymptomatic genetic testin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fd61e3b8870445c735940760ef979f4c
https://pubmed.ncbi.nlm.nih.gov/2619811
https://pubmed.ncbi.nlm.nih.gov/2619811
Autor:
M L, Franz, A B, Sokol
Publikováno v:
The Cleft palate journal. 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4b85680cb0f7ffd1c7713965903a0654
https://pubmed.ncbi.nlm.nih.gov/4504269
https://pubmed.ncbi.nlm.nih.gov/4504269