Search Results - "Ferriere, G"
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Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q
Published in Nature (London) (19-04-1990)“…Proximal spinal muscular atrophies represent the second most common fatal, autosomal recessive disorder after cystic fibrosis. The childhood form is…”
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Morphological aspects of martensite–austenite constituents in intercritical and coarse grain heat affected zones of structural steels
Published in Materials science & engineering. A, Structural materials : properties, microstructure and processing (15-11-2004)“…Thermal simulation with Gleeble was performed in order to reproduce HAZ microstructures in steels with silicon content varying between 0.003 and 0.315%…”
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Effects of interstitial oxygen on microstructure and mechanical properties of Ti-48Al-2Cr-2Nb with fully lamellar and duplex microstructures
Published in Metallurgical and materials transactions. A, Physical metallurgy and materials science (01-08-2006)“…The effect of added oxygen in the range of 1000 to 4000 wt ppm on the microstructures of a Ti-48Al-2Cr-2Nb alloy has been investigated and compared to the…”
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Relative effects of chromium and niobium on microstructure and mechanical properties as a function of oxygen content in TiAl alloys
Published in Scripta materialia (01-03-2007)“…The effects of 2 at.% chromium and niobium on microstructure and mechanical properties of Ti–48Al– x(Cr, Nb) have been investigated for alloys with different…”
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Demyelinating hereditary neuropathies in children: a morphometric and ultrastructural study
Published in Histology and histopathology (01-01-1995)“…Twenty-three cases of hereditary demyelinating neuropathies are reported, 13 with different types of hereditary motor and sensory neuropathy (HMSN) and 9 with…”
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Brain glucose utilisation in acquired childhood aphasia associated with a sylvian arachnoid cyst: recovery after shunting as demonstrated by PET
Published in Journal of neurology, neurosurgery and psychiatry (01-03-1994)“…Regional brain glucose utilisation was investigated with PET and fluorodeoxyglucose (FDG) in a case of epileptic aphasia (Landau-Kleffner syndrome) associated…”
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Morphometric studies of normal sural nerves in children
Published in Muscle & nerve (01-10-1985)“…Quantitative histologic studies of biopsies of normal sural nerves were performed on nine children aged 4 days to 17 years. Stereologic computerized procedures…”
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Redox-Active vs Redox-Innocent: A Comparison of Uranium Complexes Containing Diamine Ligands
Published in Inorganic chemistry (04-06-2018)“…Uranium complexes (MesDAE)2U(THF) (1-DAE) and Cp2U(MesDAE) (2-DAE) (MesDAE = [ArN-CH2CH2-NAr]; Ar = 2,4,6-trimethylphenyl (Mes)), bearing redox-innocent…”
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Childhood sarcoidosis presenting with prevalent muscular symptoms: report of a case
Published in European journal of pediatrics (01-04-1997)Get full text
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Distal infantile spinal muscular atrophy associated with paralysis of the diaphragm: a variant of infantile spinal muscular atrophy
Published in American journal of medical genetics (01-07-1989)“…We report the clinical, electrophysiological, and morphological observations of five infants with an unusual form of spinal muscular atrophy (SMA). In these…”
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Family "Decline" and the Subjective Well-Being of Adolescents
Published in Social indicators research (01-01-2000)“…The goal of the present study was to determine to what extent an adolescent's subjective well-being is affected when changes in family structure reach a…”
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Hyaline membrane disease: prognostic factors and medium-term follow-up
Published in European journal of pediatrics (01-09-1978)“…One hundred and twenty two cases of severe hyaline membrane disease are reported. 68 of them survived (57%). Adverse clinical, radiological and laboratory…”
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Progressive bulbar paralysis in childhood (Londe syndrome). A clinicopathological report
Published in Acta paedriatrica belgica (01-04-1979)Get more information
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Congenital hypomyelination polyneuropathy. Pathological findings compared with polyneuropathies starting later in life
Published in Brain (London, England : 1878) (01-06-1982)“…Biopsies from patients with congenital hypomyelination polyneuropathy (Group I) and with late infantile (Group II) and juvenile (Group III) forms of hereditary…”
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Congenital neuropathy with prevailing axonal changes: a clinical and histological report
Published in Acta neuropathologica (1985)“…A case of congenital neuropathy associated with an unclassified chronic brain disorder is described. Morphological findings differ from the reported congenital…”
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Familial dysautonomia in a non-Jewish girl, with histological evidence of progression in the sural nerve
Published in Developmental medicine and child neurology (01-02-1986)“…A case of typical familial dysautonomia (HSN, type III) in a non-Jewish girl is reported. The number of unmyelinated fibres was found to be reduced and sural…”
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Aqueductal stenosis in X-linked hydrocephalus: a secondary phenomenon?
Published in Developmental medicine and child neurology (01-10-1979)“…Two cases of x-linked hydrocephalus are reported. One underwent postmortem examination: serial sections of the brain stem failed to show stenosis of the…”
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A disorder of axonal development, necrotizing myopathy, cardiomyopathy, and cataracts: a new familial disease
Published in Annals of neurology (01-02-1990)“…We report severe congenital encephalopathy and profound hypotonia associated with necrotizing myopathy, cardiomyopathy, and cataracts in 3 infants, including 2…”
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Role of earthworms in the N cycle: A falsifiable assessment
Published in Soil biology & biochemistry (01-03-1997)“…Due to the great difficulty in measuring N transfers in the field, most N-cycle representations are made from laboratory data extrapolated to field earthworm…”
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