Nivelon JL - Search Results

1

Study of final height in Turner's syndrome: ethnic and genetic influences.

Rochiccioli P, David M, Malpuech G, Colle M, Limal JM, Battin J, Mariani R, Sultan C, Nivelon JL, Simonin G, et al. Rochiccioli P, et al. Among authors: nivelon jl. Acta Paediatr. 1994 Mar;83(3):305-8. doi: 10.1111/j.1651-2227.1994.tb18099.x. Acta Paediatr. 1994. PMID: 8038534 Review.

2

[Klinefelter syndrome in 1993. Results of a multicenter study on 58 cases and review of the literature].

Battin J, Malpuech G, Nivelon JL, Garandeau P, Freycon F, Sultan C, Bost M, Simonin G, Bouquier J, Rochiccioli P, et al. Battin J, et al. Among authors: nivelon jl. Ann Pediatr (Paris). 1993 Sep;40(7):432-7. Ann Pediatr (Paris). 1993. PMID: 8239394 Review. French.

3

[Discovery, in neonatal screening, of 2 families carrying a syndrome of generalized resistance to thyroid hormones].

Poitrineau P, Malpuech G, Nivelon JL, Huet F, Giraud G, François C, Carla H, Loriette Y. Poitrineau P, et al. Among authors: nivelon jl. Ann Pediatr (Paris). 1993 Sep;40(7):396-403. Ann Pediatr (Paris). 1993. PMID: 8239390 French.

4

Long-term results of GH therapy in GH-deficient children treated before 1 year of age.

Huet F, Carel JC, Nivelon JL, Chaussain JL. Huet F, et al. Among authors: nivelon jl. Eur J Endocrinol. 1999 Jan;140(1):29-34. doi: 10.1530/eje.0.1400029. Eur J Endocrinol. 1999. PMID: 10037248 Clinical Trial.

5

[Catch-up growth in growth hormone deficit children treated with GH since the first year of life].

Huet F, Carel JC, Nivelon JL, Chaussain JL. Huet F, et al. Among authors: nivelon jl. Arch Pediatr. 1998;5 Suppl 4:318S-321S. doi: 10.1016/s0929-693x(99)80183-3. Arch Pediatr. 1998. PMID: 9853076 French.

6

[Congenital generalized fibromatosis. Apropos of 3 cases].

Lauras B, Freycon F, Nivelon JL, Battin J, Gilly J, Izac M. Lauras B, et al. Among authors: nivelon jl. Pediatrie. 1976 Jun-Jul;31(4):327-35. Pediatrie. 1976. PMID: 958786 French. No abstract available.

7

[Familial benign neonatal seizures: EEG, clinical, prognosis and genetic features].

Giroud M, Soichot P, Nivelon-Chevalier A, Gouyon JB, Nivelon JL, Dumas R. Giroud M, et al. Among authors: nivelon chevalier a, nivelon jl. Neurophysiol Clin. 1989 Mar;19(1):47-54. doi: 10.1016/s0987-7053(89)80084-x. Neurophysiol Clin. 1989. PMID: 2654610 Review. French.

8

[Difficulties in diagnosis of frontal syndrome in epileptic children: clinical, diagnostic, physiopathological aspects. Apropos of 6 cases].

Septien L, Brenot M, Giroud M, Gras P, Nivelon JL, Dumas R. Septien L, et al. Among authors: nivelon jl. Pediatrie. 1992;47(4):285-90. Pediatrie. 1992. PMID: 1329013 French.

9

[Identification of temporal epilepsy in children: contribution of sphenoidal electrodes].

Septien L, Bourgeois M, Giroud M, Nivelon JL, Dumas R. Septien L, et al. Among authors: nivelon jl. Pediatrie. 1991;46(2):193-200. Pediatrie. 1991. PMID: 1646436 French.

10

[FAMILIAL SYNDROME COMBINING ATAXIA, DEAFNESS AND OLIGOPHRENIA. MYOCARDIAL SCLEROSIS WITH FATAL DEVELOPMENT IN ONE OF THE CHILDREN].

JEUNE M, TOMMASI M, FREYCON F, NIVELON JL. JEUNE M, et al. Among authors: nivelon jl. Pediatrie. 1963;18:984-7. Pediatrie. 1963. PMID: 14105581 French. No abstract available.

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