Zobrazeno 1 - 10
of 22
pro vyhledávání: '"G. D. Eng"'
Publikováno v:
Developmental Medicine & Child Neurology. 24:380-385
SUMMARY A 19-month-old Indian girl presented with a giant arterial aneurysm, associated with a spinal arteriovenous malformation, secondary bruit, failure to thrive and psychomotor developmental delay. The case is compared with the clinical and radio
Publikováno v:
Stimulus. 10:74-82
Spastische diplegie is algemeen erkend als de vorm van cerebrale verlamming, die het meeste verband houdt met premature geboorte. Vanwege de voortdurend beter wordende neonatale zorg in de ontwikkelde landen, blijven steeds meer en steeds kleinere pr
Publikováno v:
Musclenerve. 19(7)
Resurgence of neurosurgical intervention of obstetrical brachial plexus palsy prompted our review of 186 patients evaluated between 1981 and 1993, correlating clinical examination, electrodiagnosis, and functional outcome with conservative management
Publikováno v:
Archives of physical medicine and rehabilitation. 73(11)
Heterotopic ossification is the formation of ectopic bone in soft tissue, and has been reported as a rare complication in pediatric burn patients. At our hospital, two 86% body surface area burn patients developed heterotopic ossification in the shou
Autor:
P R, Bryant, G D, Eng
Publikováno v:
Archives of physical medicine and rehabilitation. 72(1)
Normal values for the soleus H-reflex were established in 83 preterm and term infants 31 to 45 weeks postconceptional age. Infants at conceptional ages 31 to 34 weeks (n = 30) had a mean H-latency (msec) of 19.2 +/- 2.16; infants 35 to 39 weeks (n =
Publikováno v:
Southern Medical Journal. 76:158-162
To determine the developmental outcome of premature infants weighing 1,750 gm or less at birth and who had grade III intraventricular hemorrhage (IVH), we followed up ten infants with IVH confirmed by computed tomography (CT) and ten CT-negative cont
Autor:
B, Bartolomei, G D, Eng
Publikováno v:
Archives of physical medicine and rehabilitation. 68(1)
Holt-Oram syndrome (HOS) is a dominant inherited disorder which causes skeletal defects of the arms and heart disease. This report describes a 2-year-old child with HOS whose skeletal anomalies affected his functional capabilities and developmental s
Publikováno v:
Archives of physical medicine and rehabilitation. 57(1)
Few prospective studies on the concomitant finding of neuropathy in juvenile diabetics exist. An ongoing study of motor and sensory nerve conduction determinations in 190 diabetic children, with sequential studies in 108 of them over an eight-year pe
Publikováno v:
Archives of neurology. 35(4)
We describe a development of a malignant hyperthermia (MH) syndrome, partially aborted by therapy, in a child with central core disease and congenital dislocating hips. Patients with central core disease appear to be more susceptible to MH; possibly
Publikováno v:
Archives of physical medicine and rehabilitation. 65(9)
Sixty patients with spinal muscular atrophy (SMA) are presented. Although the life span with Type I SMA (Werdnig-Hoffmann disease) may be short, children with the disease can be made more comfortable with appropriate medical care and parental support