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CADASIL in monozygotic twins [PDF]
Neuropathology and Applied Neurobiology, 2002 Introduction: The cause of the highly variable clinical course in CADASIL is unknown, independent of the type of mutation.Patients and clinical findings: The age of onset in the mother of monozygotic twins was 70 years. At 73 years MMSE was 22 with impairment of executive functions.
L. Bronge +4 more
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Rett syndrome in monozygotic twins
American Journal of Medical Genetics, 1988AbstractThe evolution of the Rett syndrome in 29‐year‐old twin girls is presented. Evidence for monozygosity is given together with a brief account of the problems these girls posed to their family in early childhood.
M. W. Partington +2 more
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Waldenström's Macroglobulinemia in Monozygotic Twins
Acta Medica Scandinavica, 1986ABSTRACTThis paper reports a unique familial occurrence of Waldenström's macroglobulinemia (WM) in monozygotic twins. The determination of twin monozygosity has been performed by electrophoretic and immunological typing of genetic systems (erythrocyte blood groups, leucocyte antigens and serum protein polymorphism).
D. Rochu +6 more
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Monozygotic twins with the Turner syndrome
American Journal of Obstetrics and Gynecology, 1972Abstract A monozygotic identical twin pair with the 45,XO Turner syndrome is reported. The twins were phenotypically identical, a surprisingly unusual occurrence among monozygotic twins with the Turner syndrome. Monozygotic twinning is apparently the most common form of twinning among reported patients with the Turner syndrome.
R. Neil Schimke +3 more
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Discordant abnormalities in monozygotic twins
The Journal of Pediatrics, 1965Congenital abnormalities are more often seen in monozygotic twins, especially with a monochorionic placenta, than in dizygotic twins. Although abnormalities are more frequently concordant in monozygotic than in dizygotic twins, discordance for the abnormalities among the former is strikingly frequent.
Peter Gruenwald +2 more
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Parkinson's disease in monozygotic twins
Annals of Neurology, 1986AbstractRecent studies of twins have demonstrated an unexpectedly low concordance of Parkinson's disease in monozygotic twins. Only two monozygotic twin pairs concordant for it have been reported. However, both pairs were atypical because of an early age at onset and other unusual features.
Joseph Jankovic, Avi Reches
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1954
Publisher Summary Despite the fact that more than two decades have passed since Kronacher began his studies on cattle twins, no single test or series of tests yet exists through which it would be possible to distinguish between monozygotic and dizygotic cattle twins in an objective manner.
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Publisher Summary Despite the fact that more than two decades have passed since Kronacher began his studies on cattle twins, no single test or series of tests yet exists through which it would be possible to distinguish between monozygotic and dizygotic cattle twins in an objective manner.
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Birdshot retinochoroidopathy in monozygotic twins
Acta Ophthalmologica, 1992Abstract Birdshot retinochoroidopathy is a rare ocular disorder which was named and delineated as a separate clinical entity by Ryan & Maumenee in 1980. We diagnosed birdshot retinochoroidopathy in a monozygotic pair of twins, who were affected with a time interval of 12 years, respectively.
Marianne Fich, Thomas Rosenberg
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Videokeratography of Keratoconus in Monozygotic Twins
Journal of Refractive Surgery, 1996ABSTRACT PURPOSE: To determine the corneal topographic appearance in a pair of monozygotic twins and family members of the twins because one of the twins had keratoconus and the other appeared normal by clinical examination. METHODS: Clinical examination and videokeratography (Topographic Modeling System, Tomey) of the patient, his ...
William W Ko +5 more
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Nongoitrous Cretinism in Monozygotic Twins
Archives of Pediatrics & Adolescent Medicine, 1969NONGOITROUS CRETINISM is presumed to be nongenetically determined, since it usually occurs as an isolated case within a family pedigree. Recent reports of concordance for this disorder among monozygotic twins 1,2 and familial instances 1,3-5 lend some support toward a genetic etiology.
James W. Bass, Alva L. Strickland
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