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See detailCerebral subarachnoid blood migration consecutive to a lumbar haematoma after spinal anaesthesia
Hans, Grégory ULg; Senard, Marc ULg; Ledoux, Didier ULg et al

in Acta Anaesthesiologica Scandinavica (2008), 52

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See detailCerebrospinal fluid level of protein S100 beta in healthy horse : a preliminary study
Lopez, D; De Moffarts, Brieuc; Delguste, Catherine ULg et al

in Tierärztliche Praxis Kleintiere (2004)

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See detailCerebrospinal Fluid Collection Tubes: a critical issue for Alzheimer Disease diagnosis
Perret-Liaudet, Armand; Pelpel, Mathieu; Tholance, Yannick et al

in Clinical Chemistry (2012), 58

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See detailCerebrospinal fluid IgG and IgM indexes as indicators of active neurosyphilis
Hische, EAH; Tutuarima, JA; Wolters, EC et al

in Clinical Chemistry (1988), 34

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See detailCerebrospinal fluid neurophysins in affective illness and schizophrenia
Linkowski, Paul; Geenen, Vincent ULg; Kerkhofs, Myriam et al

in European Archives of Psychiatry and Neurological Sciences (1984), 234

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See detailCerebrospinal fluid pterins and folates in Aicardi-Goutières syndrome: A new phenotype
Blau, N.; Bonafé, L.; Krägeloh-Mann, I. et al

in Neurology (2003), 61(5), 642-647

Objective: To describe three unrelated children with a distinctive variant of Aicardi-Goutières syndrome (AGS) characterized by microcephaly, severe mental and motor retardation, dyskinesia or spasticity ... [more ▼]

Objective: To describe three unrelated children with a distinctive variant of Aicardi-Goutières syndrome (AGS) characterized by microcephaly, severe mental and motor retardation, dyskinesia or spasticity, and occasional seizures. Results: Neuroimaging showed bilateral calcification of basal ganglia and white matter. CSF glucose, protein, cell count, and interferon alpha were normal. Abnormal CSF findings included extremely high neopterin (293 to 814 nmol/L; normal 12 to 30 nmol/L) and biopterin (226 to 416 nmol/L; normal 15 to 40 nmol/L) combined with lowered 5-methyltetrahydrofolate (23 to 48 nmol/L; normal 64 to 182 nmol/L) concentrations in two patients. The absence of pleocytosis and normal CSF interferon alpha was a characteristic finding compared to the classic AGS syndrome. Genetic and enzymatic tests excluded disorders of tetrahydrobiopterin metabolism, including mutation analysis of GTP cyclohydrolase feed-back regulatory protein. CSF investigations in three patients with classic AGS also showed increased pterins and partially lowered folate levels. Conclusions: Intrathecal overproduction of pterins is the first biochemical abnormality identified in patients with AGS variants. Long-term substitution with folinic acid (2-4 mg/kg/day) resulted in substantial clinical recovery with normalization of CSF folates and pterins in one patient and clinical improvement in another. The underlying defect remains unknown. [less ▲]

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See detailCerebrotendinous xanthomatosis, a rare, severe, but treatable metabolic disorder
Delstanche, S.; Deflandre, T.; Otto, B. et al

in Revue Médicale de Liège (2013), 68(4), 171-6

Cerebrotendinous xanthomatosis (CTX) is a rare and treatable autosomal recessive disease. The diagnosis should be suspected in the presence of a suggestive clinical triad characterized by early-onset ... [more ▼]

Cerebrotendinous xanthomatosis (CTX) is a rare and treatable autosomal recessive disease. The diagnosis should be suspected in the presence of a suggestive clinical triad characterized by early-onset cataract, tendinous xanthomata and neurological symptoms and signs, notably cerebellar ataxia, mental retardation and pyramidal syndrome.The diagnosis is confirmed by demonstrating an increased blood level of cholestanol, or/and by molecular genetic analysis.In typical cases, brain MRI shows bilateral hyperintensity of the cerebellar nucleus dentatus together with cerebral atrophy and leukoencephalopathy. The treatment is based on the administration of chenodeoxycholic acid. The aim is to restore the negative feedback on the enzymatic cascade altered by mutation in the gene CYP27 which induces a 27-hydroxylase deficiency [less ▲]

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See detailCérémonie d'«arrestation» du roi en pays Bamiléké
Schmitz, Serge ULg

Article for general public (2012)

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See detailCérès vue par Dawn
Manfroid, Jean ULg

Article for general public (2015)

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See detailCerium: The lithium substitute in post-AGB stars
Reyniers, M.; Winckel, H. V.; Biémont, Emile ULg et al

in Astronomy and Astrophysics (2002), 395(2), 35-38

In this letter we present an alternative identification for the line detected in the spectra of s-process enriched low-mass post-AGB stars around 6708 Angstrom and which was interpreted in the literature ... [more ▼]

In this letter we present an alternative identification for the line detected in the spectra of s-process enriched low-mass post-AGB stars around 6708 Angstrom and which was interpreted in the literature as due to Li. Newly released line lists of lanthanide species reveal, however, the likely identification of the line to be due to a Ce II transition. We argue that this identification is consistent with the Ce abundance of all the objects discussed in the literature and conclude that in none of the low-mass s-process enriched post-AGB stars there is indication for Li-production. [less ▲]

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See detailTHE CERT project : final report
Denis, Brigitte ULg

Report (1995)

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See detailUn certain regard (1): des pierres levées vers le Ciel
Nazé, Yaël ULg

Article for general public (2001)

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See detailUn certain regard (2): la sagesse orientale
Nazé, Yaël ULg

Article for general public (2001)

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See detailUn certain regard (3): au coeur du pouvoir
Nazé, Yaël ULg

Article for general public (2001)

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See detailUne certaine idée du bonheur
Droixhe, Daniel ULg

in Droixhe, Daniel (Ed.) L'Esprit des journaux : un périodique europée au XVIIIe siècle (2009, October 12)

Detailed reference viewed: 87 (8 ULg)