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Abnormal meiotic recombination in infertile men and its association with sperm aneuploidy.
- K. Ferguson, E. Wong, V. Chow, M. Nigro, S. Ma
- Medicine, Biology
- Human molecular genetics
- 1 December 2007
Defects in early meiotic events are thought to play a critical role in male infertility; however, little is known regarding the relationship between early meiotic events and the chromosomal… Expand
Adjunctive therapy with oxcarbazepine in children with partial seizures
Objective: To evaluate the safety and efficacy of oxcarbazepine (OXC) as adjunctive therapy in children with inadequately controlled partial seizures on one or two concomitant antiepileptic drugs… Expand
Diagnosis and treatment of prostatitis in Canada.
OBJECTIVES There is a general consensus among physicians that the present management of chronic prostatitis is dismal. We undertook a survey of Canadian primary care physicians (PCPs) and urologists… Expand
Central nervous system lesions in childhood leukemia
Central nervous system (CNS) lesions were found in 85 of 91 children with acute leukemia. Cerebral atrophy was the most common lesion, occurring in 65 percent. Atrophy was most severe in children… Expand
Autonomic dysreflexia severity during urodynamics and cystoscopy in individuals with spinal cord injury
Study Design:Retrospective chart review.Objective:To compare autonomic dysreflexia (AD) severity during urodynamics and cystoscopy in individuals with spinal cord injury (SCI).Setting:Outpatient… Expand
Impaired NADH-CoQ reductase activity in a child with moyamoya syndrome.
- S. Kotagal, P. L. Peterson, M. Martens, C. Lee, M. Nigro, C. Archer
- Pediatric neurology
- 1 July 1988
A 33-month-old boy with recurrent stroke-like episodes had angiographic features characteristic of moyamoya syndrome. Mitochondrial encephalomyopathy was suspected because of lactic acidosis and… Expand
A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings
- C. Mauro, G. Giaccone, +9 authors G. Puoti
- Biology, Medicine
- Journal of Neurology, Neurosurgery, and…
- 14 November 2008
A young man, presenting with early onset of personality and behavioural changes followed by slowly progressive cognitive impairment associated with marked bi-parietal cerebral atrophy, was found to… Expand
Deferoxamine followed by cyclophosphamide, etoposide, carboplatin, thiotepa, induction regimen in advanced neuroblastoma: preliminary results. Italian Neuroblastoma Cooperative Group.
Based upon phase I and II studies of deferoxamine alone and in combination with cytotoxic agents cyclophosphamide, etoposide, carboplatin, and thiotepa (D-CECaT), we initiated a single arm… Expand
Peroxisomal defects in neonatal-onset and X-linked adrenoleukodystrophies.
Accumulation of very long chain fatty acids in X-linked and neonatal forms of adrenoleukodystrophy (ALD) appears to be a consequence of deficient peroxisomal oxidation of very long chain fatty acids.… Expand
Progressive Dystonia in a Child With Chromosome 18p Deletion, Treated With Intrathecal Baclofen
We report a case of dystonia with a partial deletion of the short arm (p) of chromosome 18 and androgen insensitivity Neurologic findings in the 18p syndrome are reported to include mental… Expand