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Allo-immune membranous nephropathy and recombinant aryl sulfatase replacement therapy: a need for tolerance induction therapy.
- H. Debiec, V. Valayannopoulos, P. Ronco
- Medicine, BiologyJournal of the American Society of Nephrology…
- 1 April 2014
This work identifies a new antigen responsible for secondary membranous nephropathy in a patient with mucopolysaccharidosis type VI caused by aryl sulfatase B (ASB) deficiency and concludes that the allo-immune response to the recombinant rhASB caused the nephrotic syndrome.
Infection à parechovirus du jeune nourrisson
Infection multifocale invasive à Kingella kingae
[Lipomas of the mesentery in young children].
A case which underlines the difficulty of establishing the diagnosis of Lipomas of the small bowel and mesentery before exploratory laparotomy is reported, which is exceedingly rare in young pediatric patients.
[Multifocal invasive Kingella kingae infection].
- H. Sarda, D. Ghazali, M. Thibault, F. Leturdu, C. Adams, H. Le Loc'h
- Medicine, BiologyArchives de pediatrie : organe officiel de la…
The tropism of Kingella kingae is essentially osteoarticular and cardiac as shown by the cases reported in the literature, and its susceptibility to antibiotics explains the frequent favourable outcome.
[Neonatal parechovirus infection, fever, irritability and myositis].
[Syncope after niaprazine (Nopron)].
11-Deoxycorticosterone Producing Adrenal Hyperplasia as a Very Unusual Cause of Endocrine Hypertension: Case Report and Systematic Review of the Literature
11-deoxycorticosterone-producing adrenal lesions are very rare, affecting mostly middle-aged women with a primary aldosteronism-like clinical presentation and carcinoma is the most frequent histological diagnosis.
[Efficacy and good tolerance of omeprazole in a case of refractory ulcerative esophagitis in the child].
[Neonatal adrenoleukodystrophy. Apropos of 3 cases in siblings].
- H. Sarda, V. Henry, H. Le Loc'h, P. Aubourg, B. Poll-The, J. Saudubray
- Medicine, PsychologyAnnales de pediatrie
Differences with X-linked adrenoleukodystrophy include genetic inheritance, which is autosomal recessive, a more severe prognosis, and presence of multiple peroxisome enzyme deficiencies that justify classification alongside the Zellweger syndrome among the peroxISome disorders.