๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Heterogeneity of prenatal onset hydrocephalus: Management and counseling implications

โœ Scribed by Williamson, Roger A. ;Schauberger, Charles W. ;Varner, Michael W. ;Aschenbrener, Carol A. ;Opitz, John M.


Publisher
John Wiley and Sons
Year
1984
Tongue
English
Weight
561 KB
Volume
17
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Familial hydrocephalus of prenatal onset
โœ Zlotogora, Joรซl ;Sagi, Michal ;Cohen, Tirza ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 223 KB
Spectrum of early-onset and late-onset b
โœ Sang-Oh Lee; Seung H. Kang; Rima C. Abdel-Massih; Robert A. Brown; Raymund R. Ra ๐Ÿ“‚ Article ๐Ÿ“… 2011 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 111 KB

Bacteremia is a significant cause of morbidity and mortality after liver transplantation. The characterization of the microbiological spectrum of bacteremia after liver transplantation may help physicians in choosing the initial empirical antimicrobial therapy for patients presenting with sepsis. Th

47,XXY (KLINEFELTER SYNDROME) AND 47,XYY
โœ L. ABRAMSKY; J. CHAPPLE ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 145 KB

Cytogenetic surveys of neonates have found that approximately one boy in 500 is born with an extra sex chromosome. Some of these boys are now being diagnosed when prenatal karyotyping is done for the detection of Down syndrome and other major aneuploidies. This study estimates what proportion of tho

Prenatal diagnosis of reversible cardiac
โœ Dr. Diane C. Crawford; David P. Drake; Dominic Kwaitkowski; Michael G. Chapman; ๐Ÿ“‚ Article ๐Ÿ“… 1986 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 323 KB

Ultrasonic prenatal diagnosis of congenital diaphragmatic hernia has been reported by several centers. 1-5 Identification of abdominal organs in the thoracic cavity, above the diaphragm and adjacent to the fetal heart, is a reliable indicator of congenital diaphragmatic hernia. In some instances the

Functional analysis reveals splicing mut
โœ Nathalie Roux-Buisson; John Rendu; Isabelle Denjoy; Pascale Guicheney; Alice Gol ๐Ÿ“‚ Article ๐Ÿ“… 2011 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 179 KB

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare and severe arrhythmogenic disorder. Although usually transmitted in a recessive form, few cases of dominant mutations have been reported. Thirteen mutations in the CASQ2 gene have been reported so far in association with CPVT. We