Hardelin JP - Search Results

1

Xp22.3 deletions in isolated familial Kallmann's syndrome.

Hardelin JP, Levilliers J, Young J, Pholsena M, Legouis R, Kirk J, Bouloux P, Petit C, Schaison G. Hardelin JP, et al. J Clin Endocrinol Metab. 1993 Apr;76(4):827-31. doi: 10.1210/jcem.76.4.8473391. J Clin Endocrinol Metab. 1993. PMID: 8473391

2

X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene.

Hardelin JP, Levilliers J, del Castillo I, Cohen-Salmon M, Legouis R, Blanchard S, Compain S, Bouloux P, Kirk J, Moraine C, et al. Hardelin JP, et al. Proc Natl Acad Sci U S A. 1992 Sep 1;89(17):8190-4. doi: 10.1073/pnas.89.17.8190. Proc Natl Acad Sci U S A. 1992. PMID: 1518845 Free PMC article.

3

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules.

Legouis R, Hardelin JP, Levilliers J, Claverie JM, Compain S, Wunderle V, Millasseau P, Le Paslier D, Cohen D, Caterina D, et al. Legouis R, et al. Among authors: hardelin jp. Cell. 1991 Oct 18;67(2):423-35. doi: 10.1016/0092-8674(91)90193-3. Cell. 1991. PMID: 1913827

4

A molecular approach to the pathophysiology of the X chromosome-linked Kallmann's syndrome.

Hardelin JP, Petit C. Hardelin JP, et al. Baillieres Clin Endocrinol Metab. 1995 Jul;9(3):489-507. doi: 10.1016/s0950-351x(95)80553-2. Baillieres Clin Endocrinol Metab. 1995. PMID: 7575329 Review.

5

Early expression of the KAL gene during embryonic development of the chick.

Legouis R, Hardelin JP, Petit C, Ayer-Le Lièvre C. Legouis R, et al. Among authors: hardelin jp. Anat Embryol (Berl). 1994 Dec;190(6):549-62. doi: 10.1007/BF00190105. Anat Embryol (Berl). 1994. PMID: 7893008

6

Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome.

Hardelin JP, Levilliers J, Blanchard S, Carel JC, Leutenegger M, Pinard-Bertelletto JP, Bouloux P, Petit C. Hardelin JP, et al. Hum Mol Genet. 1993 Apr;2(4):373-7. doi: 10.1093/hmg/2.4.373. Hum Mol Genet. 1993. PMID: 8504298

7

Kallmann syndrome.

Hardelin JP, Soussi-Yanicostas N, Ardouin O, Levilliers J, Petit C. Hardelin JP, et al. Adv Otorhinolaryngol. 2000;56:268-74. doi: 10.1159/000059073. Adv Otorhinolaryngol. 2000. PMID: 10868244 Review. No abstract available.

8

Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous system.

Soussi-Yanicostas N, Hardelin JP, Arroyo-Jimenez MM, Ardouin O, Legouis R, Levilliers J, Traincard F, Betton JM, Cabanié L, Petit C. Soussi-Yanicostas N, et al. Among authors: hardelin jp. J Cell Sci. 1996 Jul;109 ( Pt 7):1749-57. doi: 10.1242/jcs.109.7.1749. J Cell Sci. 1996. PMID: 8832397

9

Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific manner.

Soussi-Yanicostas N, Faivre-Sarrailh C, Hardelin JP, Levilliers J, Rougon G, Petit C. Soussi-Yanicostas N, et al. Among authors: hardelin jp. J Cell Sci. 1998 Oct;111 ( Pt 19):2953-65. doi: 10.1242/jcs.111.19.2953. J Cell Sci. 1998. PMID: 9730987

10

Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndrome.

Hardelin JP, Soussi-Yanicostas N, Levilliers J, Kalatzis V, Abdelhak S, Cohen-Salmon M, Petit C. Hardelin JP, et al. Adv Nephrol Necker Hosp. 1998;28:419-28. Adv Nephrol Necker Hosp. 1998. PMID: 9890002 Review. No abstract available.

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