Zobrazeno 1 - 6
of 6
pro vyhledávání: '"R D, Bellah"'
Autor:
R D Bellah, M K Goyal
Publikováno v:
Journal of Ultrasound in Medicine. 12:119-122
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96c2790bac11d48f3e710d4b4b44026a
https://doi.org/10.7863/jum.1993.12.2.119
https://doi.org/10.7863/jum.1993.12.2.119
Autor:
M. E. C. Boulden, Harcke Ht, R. J. Padman, Gerald A. Mandell, N. H. Sherman, R. D. Bellah, K. W. Mcnicholas
Publikováno v:
Radiology. 186:383-386
Nineteen infants aged 2 months to 2.5 years, first seen predominantly with stridor, were noted to have intermittent soft-tissue mass effect in the upper airway during routine evaluation with fluoroscopic or radiographic methods. The cervicothoracic t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3a36931336fe7237e8306d6ed7e4960
https://doi.org/10.1148/radiology.186.2.8421739
https://doi.org/10.1148/radiology.186.2.8421739
Autor:
B S, Kaplan, R D, Bellah
Publikováno v:
American journal of medical genetics. 87(5)
We describe two brothers with variable expression of a unique syndrome. One sib has postaxial polydactyly of the right hand and feet, two digits on the left hand (a thumb and first digit), bilateral ulnar ray dysgenesis, ectrodactyly of one hand, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a33b7dac97491d5569547bfd415e77b0
https://pubmed.ncbi.nlm.nih.gov/10594882
https://pubmed.ncbi.nlm.nih.gov/10594882
Publikováno v:
American journal of medical genetics. 78(5)
The Hajdu-Cheney syndrome (HCS) is a rare autosomal dominant disorder. It comprises a coarse face, short neck, hirsutism, joint laxity, and normal intelligence. Bone dysplasias, include acro-osteolysis, bathrocephaly, and vertebral anomalies. In 1988
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1df93dc3bbf873230351558a1b38c600
https://pubmed.ncbi.nlm.nih.gov/9714016
https://pubmed.ncbi.nlm.nih.gov/9714016
Publikováno v:
Pediatric Radiology. 19:119-121
Several authors have reported an association between neuroblastoma and congenital heart disease; others contend that, unlike specific well-known associations between malignancy and congenital defects (Wilm's tumor and aniridia, leukemia and Down's sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::020281a224e7a9aa9d041abd582a3bc2
https://doi.org/10.1007/bf02387900
https://doi.org/10.1007/bf02387900
Publikováno v:
Pediatric Radiology. 20:115-117
The authors report a congenital portosystemic shunt which was detected with ultrasound in an infant with a fatal congenital hypertrophic cardiomyopathy. An aberration in primitive vitelline venous development may have contributed to the formation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::579e22c0e2dcafe8228bf2fb23750bea
https://doi.org/10.1007/bf02010654
https://doi.org/10.1007/bf02010654