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Items: 18

1.

[Pharmacological chaperones: a potential therapeutic treatment for conformational diseases].

Mendre C, Mouillac B.

Med Sci (Paris). 2010 Jun-Jul;26(6-7):627-35. doi: 10.1051/medsci/2010266-7627. Review. French.

2.

[A discussion about key issues in retinal prosthesis].

Peng C, Xia L, Wang X, Zheng E.

Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2009 Jun;26(3):671-5. Review. Chinese.

PMID:
19634695
3.

Deafness genes in Israel: implications for diagnostics in the clinic.

Brownstein Z, Avraham KB.

Pediatr Res. 2009 Aug;66(2):128-34. doi: 10.1203/PDR.0b013e3181aabd7f. Review.

PMID:
19390476
4.

The effect of oxygen and light on the structure and function of the neonatal rat retina.

Dorfman AL, Joly S, Hardy P, Chemtob S, Lachapelle P.

Doc Ophthalmol. 2009 Feb;118(1):37-54. doi: 10.1007/s10633-008-9128-7. Epub 2008 May 16. Review.

PMID:
18483821
5.

[Non-syndromic hereditary hearing impairment].

Birkenhäger R, Aschendorff A, Schipper J, Laszig R.

Laryngorhinootologie. 2007 Apr;86(4):299-309; quiz 310-3. Review. German.

PMID:
17407011
6.

[Genetic deafness].

Marcolla A, Bouchetemble P, Lerosey Y, Marie JP, Dehesdin D.

Ann Otolaryngol Chir Cervicofac. 2006 Jun;123(3):143-7. Review. French.

PMID:
16840903
7.

Clinical disorders affecting mesopic vision.

Petzold A, Plant GT.

Ophthalmic Physiol Opt. 2006 May;26(3):326-41. Review.

PMID:
16684159
8.

RPGRIP1 is mutated in Leber congenital amaurosis: a mini-review.

Koenekoop RK.

Ophthalmic Genet. 2005 Dec;26(4):175-9. Review.

PMID:
16352478
9.

Progress toward understanding the genetic and biochemical mechanisms of inherited photoreceptor degenerations.

Pacione LR, Szego MJ, Ikeda S, Nishina PM, McInnes RR.

Annu Rev Neurosci. 2003;26:657-700. Review.

PMID:
14527271
10.

[Macular dystrophies].

Souied E, Kaplan J, Coscas G, Soubrane G.

J Fr Ophtalmol. 2003 Sep;26(7):743-62. Review. French.

11.

[Syndromic hereditary deafness. Usher's syndrome. Oto-neurologic and genetic factors].

Espinós C, Pérez-Garrigues H, Beneyto M, Vilela C, Rodrigo O, Nájera C.

An Otorrinolaringol Ibero Am. 1999;26(1):83-95. Review. Spanish.

PMID:
10091368
12.

[Electroretinogram: technique and clinical applications].

Vilela C, Cortés V, Vallet M.

Rev Neurol. 1998 Mar;26(151):444-7. Review. Spanish.

PMID:
9585960
13.

Mitochondrial encephalomyopathy and hypoparathyroidism associated with a duplication and a deletion of mitochondrial deoxyribonucleic acid.

Tengan CH, Kiyomoto BH, Rocha MS, Tavares VL, Gabbai AA, Moraes CT.

J Clin Endocrinol Metab. 1998 Jan;83(1):125-9. Review.

PMID:
9435428
14.

Genealogy, natural history, and phenotype of Alström syndrome in a large Acadian kindred and three additional families.

Marshall JD, Ludman MD, Shea SE, Salisbury SR, Willi SM, LaRoche RG, Nishina PM.

Am J Med Genet. 1997 Dec 12;73(2):150-61. Review.

PMID:
9409865
15.

Molecular genetics of human visual pigments.

Nathans J, Merbs SL, Sung CH, Weitz CJ, Wang Y.

Annu Rev Genet. 1992;26:403-24. Review. No abstract available.

PMID:
1482119
16.

Clinical implications of guanine nucleotide-binding proteins as receptor-effector couplers.

Spiegel AM, Gierschik P, Levine MA, Downs RW Jr.

N Engl J Med. 1985 Jan 3;312(1):26-33. Review. No abstract available.

PMID:
2856889
17.

X-linkage in manic-depressive illness.

Cadoret RJ, Winokur G.

Annu Rev Med. 1975;26:21-5. Review. No abstract available.

PMID:
1096758
18.

[RETINITIS PIGMENTOSA. ETIOPATHOGENETIC AND THERAPEUTIC ASPECTS].

MASTRANGELI W.

Clin Ter. 1963 Aug 15;26:255-76. Review. Italian. No abstract available.

PMID:
14050047
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