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A French experience of type 3 Gaucher disease: Phenotypic diversity and neurological outcome of 10 patients.
Brain Dev. 2011 Feb;33(2):131-9. doi: 10.1016/j.braindev.2010.02.005. Epub 2010 Mar 21.
Brain Dev. 2011.
PMID: 20307947
[Severe anorexia in infants in Reunion: a new autosomal recessive disease?].
Renouil M, Fourmaintraux A, Cartault F, Rodriguez D, Razafinarivo-Schoreitz S, Chaurand G, Wendling C, Bangui A, Ponsot G.
Renouil M, et al. Among authors: chaurand g.
Arch Pediatr. 1999 Jul;6(7):725-34. doi: 10.1016/s0929-693x(99)80354-6.
Arch Pediatr. 1999.
PMID: 10429812
French.
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[MELAS syndrome in a five year-old child: clinical, biological and genetic characteristics].
Edmar A, Lombès A, Renouil M, Bangui A, Lamblin D, Boumahni B, Chaurand G, Mariette JB, Fourmaintraux A, Vallee L.
Edmar A, et al. Among authors: chaurand g.
Arch Pediatr. 1998 Sep;5(9):1000-3. doi: 10.1016/s0929-693x(98)80012-2.
Arch Pediatr. 1998.
PMID: 9789633
French.
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[Type anti-SGPG antiglycolipid antibodies and Miller Fisher syndrome].
Edmar A, Boumahni B, Djemili S, Chaurand G, Renouil M, Bangui A, Mallet EC, Mariette JB, Fourmaintraux A.
Edmar A, et al. Among authors: chaurand g.
Arch Pediatr. 1998 Apr;5(4):460-1.
Arch Pediatr. 1998.
PMID: 9759173
French.
No abstract available.
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