Maurin N - Search Results

1

CpG dinucleotides are mutation hot spots in phenylketonuria.

Abadie V, Lyonnet S, Maurin N, Berthelon M, Caillaud C, Giraud F, Mattei JF, Rey J, Rey F, Munnich A. Abadie V, et al. Among authors: maurin n. Genomics. 1989 Nov;5(4):936-9. doi: 10.1016/0888-7543(89)90137-7. Genomics. 1989. PMID: 2574153

2

[A rare cause of neonatal hyperphenylalaninemia: tyrosinemia type I].

Sarles J, Maurin N, Giraud F. Sarles J, et al. Among authors: maurin n. Pediatrie. 1992;47(12):809-11. Pediatrie. 1992. PMID: 1338924 French.

3

[Pregnancy and the child of a mother with phenylketonuria].

Abadie V, Depondt E, Farriaux JP, Lepercq J, Lyonnet S, Maurin N, Ogier de Baulny H, Vidailhet M. Abadie V, et al. Among authors: maurin n. Arch Pediatr. 1996 May;3(5):489-6. doi: 10.1016/0929-693x(96)86411-6. Arch Pediatr. 1996. PMID: 8763723 Review. French.

4

Neonatal screening and long-term follow-up of phenylketonuria: the French database.

Abadie V, Berthelot J, Feillet F, Maurin N, Mercier A, de Baulny HO, de Parscau L. Abadie V, et al. Among authors: maurin n. Early Hum Dev. 2001 Dec;65(2):149-58. doi: 10.1016/s0378-3782(01)00223-7. Early Hum Dev. 2001. PMID: 11641035

5

[Management of phenylketonuria and hyperphenylalaninemia: the French guidelines].

Abadie V, Berthelot J, Feillet F, Maurin N, Mercier A, Ogier de Baulny H, de Parscau L; Association française pour le dépistage et la prévention des handicaps de l'enfant (AFDPHE). Abadie V, et al. Among authors: maurin n. Arch Pediatr. 2005 May;12(5):594-601. doi: 10.1016/j.arcped.2005.02.004. Arch Pediatr. 2005. PMID: 15885553 Review. French.

6

[Neonatal screening for phenylketonuria and hypothyroidism. An optimizing system].

Reviron D, Auquier P, Giusiano B, Maurin N, Sambuc R, Giraud F. Reviron D, et al. Among authors: maurin n. Arch Fr Pediatr. 1990 Apr;47(4):255-6. Arch Fr Pediatr. 1990. PMID: 2363612 French.

7

Maternal phenylketonuria: the French survey.

Feillet F, Abadie V, Berthelot J, Maurin N, Ogier H, Vidailhet M, Farriaux JP, de Parscau L. Feillet F, et al. Among authors: maurin n. Eur J Pediatr. 2004 Sep;163(9):540-6. doi: 10.1007/s00431-004-1482-1. Epub 2004 Jul 6. Eur J Pediatr. 2004. PMID: 15241684

8

[The register of stillbirths in Bouches-du-Rhône: evaluation after 3 years in operation].

Aymé S, Julian C, Maurin N, Gambarelli D, Sudan N, Giraud F. Aymé S, et al. Among authors: maurin n. J Genet Hum. 1985 Sep;33(3-4):265-74. J Genet Hum. 1985. PMID: 4056749 French.

9

[Neonatal screening for phenylketonuria and hypothyroidism].

Maurin N, Sarles J. Maurin N, et al. Rev Prat. 2000 Oct 1;50(15):1728-31. Rev Prat. 2000. PMID: 11116617 French. No abstract available.

10

[Evaluation of 47,213 infants in neonatal screening for cystic fibrosis, using pancreatitis-associated protein and immunoreactive trypsinogen assays].

Barthellemy S, Maurin N, Roussey M, Férec C, Murolo S, Berthézène P, Iovanna JL, Dagorn JC, Sarles J. Barthellemy S, et al. Among authors: maurin n. Arch Pediatr. 2001 Mar;8(3):275-81. doi: 10.1016/s0929-693x(00)00194-9. Arch Pediatr. 2001. PMID: 11270251 French.

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