نتایج جستجو برای: intrafamilial

تعداد نتایج: 714  

Journal: :Journal of child sexual abuse 2013
Hilary Cahalane Gemma Parker Simon Duff

There is a dearth of current empirical research exploring the experiences of nonoffending partners, or women whose partners have perpetrated child sexual abuse. Existing literature is dated and focuses disproportionately on intrafamilial abuse. This research explores how nonoffending partners construct and understand their experiences using thematic analysis within a social constructionist fram...

2018
Kazuki Ocho Masaya Iwamuro Kou Hasegawa Hideharu Hagiya Kammei Rai Tetsuya Yumoto Fumio Otsuka

A previously healthy 31-year-old man was referred to us with refractory septic shock accompanied by bilateral conjunctival congestion and erythema of his right lower limb. Nine days after admission, he had bilateral desquamation of the fingertips, and his presentation satisfied the criteria for Kawasaki disease. A serological examination was positive for Yersinia pseudotuberculosis, and he was ...

Journal: :Journal of chronic diseases 1969
S Cobb S V Kasl J R French G Nörstebö

SOME years ago the senior author publicly expressed [l] the hypothesis that women with rheumatoid arthritis should, with undue frequency, be married to men with peptic ulcers. The reason given for this speculation was that it seemed likely that the hostility in these marriages [2, 31 would leave unmet the husbands’ needs for emotional support and the wives’ needs for ego support. When in the co...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2005
S Benedetti E Bertini S Iannaccone C Angelini M Trisciani D Toniolo B Sferrazza P Carrera G Comi M Ferrari A Quattrini S C Previtali

The coexistence of neurogenic and myogenic features in scapuloperoneal syndrome is rarely ascribed to a single gene. Defects in the nuclear envelope protein lamin A/C, encoded by the LMNA gene, have been shown to be associated with a variety of disorders affecting mainly the muscular and adipose tissues and, more recently, with autosomal recessive Charcot-Marie-Tooth type 2 neuropathy. This rep...

Journal: :British medical journal 1977
A Heiberg J Slack

In a combined Norwegian and British study of the age at death from coronary heart disease of heterozygotes for familial hypercholesterolaemia (FH) the correlation coefficients within families for 43 sib pairs was 0-70 and for 14 first cousin pairs 0-61. There was no significant correlation between the age at death and serum cholesterol concentration in either series. The intrafamilial correlati...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1989
G De Michele A Filla F Barbieri A Perretti L Santoro L Trombetta F Santorelli G Campanella

The Quebec Cooperative Study on Friedreich's ataxia required an onset before age 20 as an obligatory criterion of Friedreich's disease (FD). Harding included patients with onset before 25 years. We studied nine patients with FD phenotype but with onset ranging from 21 to 29 years (mean 24.4). Statistical analysis of the distribution and intrafamilial variation of onset age suggests that late on...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2005
M B Sánchez-Arjona J J Rodríguez-Uranga M Giles-Lima R Fernández-García I Chinchón-Lara G Antiñolo J Bautista-Lorite

A Spanish family is reported with dystrophinopathy of myalgia and cramps syndrome type. There were five affected males and three females, and also six asymptomatic carriers. Muscle biopsy showed a dystrophic pattern, but immunohistochemistry carried out with three anti-dystrophin antibodies was normal. Dystrophin analysis by western blot revealed a dystrophin of reduced quantity and molecular w...

2016
Niklas Wahlberg Carlos Peña Milla Ahola Christopher W. Wheat Jadranka Rota

We report primer pairs for 30 new gene regions in the nuclear genomes of Lepidoptera that can be amplified using a standard PCR protocol. The new primers were tested across diverse Lepidoptera, including nonditrysians and a wide selection of ditrysians. These new gene regions give a total of 11,043 bp of DNA sequence data and they show similar variability to traditionally used nuclear gene regi...

Journal: :Journal of medical genetics 1995
D J Bunyan J Shea-Simonds A C Reck D Finnis D M Eccles

Nine new causative mutations and seven previously characterised mutations of the APC gene of patients with familial adenomatous polyposis (FAP) were analysed for any genotype-phenotype correlations. The only clear genotype-phenotype correlation found was between the position of the mutation site and the presence or absence of congenital hypertrophy of the retinal pigment epithelium (CHRPE). A m...

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