Format
Sort by

Send to

Choose Destination

Search results

Items: 20

1.

[Take the time: primary healthcare for people with intellectual disabilities].

Bakker-van Gijssel EJ, Lucassen PL.

Ned Tijdschr Geneeskd. 2014;158:A7995. Review. Dutch.

PMID:
25370948
2.

The diverse genetic landscape of neurodevelopmental disorders.

Hu WF, Chahrour MH, Walsh CA.

Annu Rev Genomics Hum Genet. 2014;15:195-213. doi: 10.1146/annurev-genom-090413-025600. Review.

PMID:
25184530
3.

Surgical treatment for kyphoscoliosis in Cohen syndrome.

Imagama S, Tsuji T, Ohara T, Katayama Y, Goto M, Ishiguro N, Kawakami N.

Nagoya J Med Sci. 2013 Aug;75(3-4):279-86. Review.

4.

Clinical variability of genetic isolates of Cohen syndrome.

Douzgou S, Petersen MB.

Clin Genet. 2011 Jun;79(6):501-6. doi: 10.1111/j.1399-0004.2011.01669.x. Epub 2011 Apr 7. Review.

PMID:
21418059
5.

[Myopia in systemic disorders].

Mrugacz M, Rydzanicz M, Frajdenberg A, Podfigurna-Musielak M, Gajecka M.

Klin Oczna. 2009;111(1-3):84-8. Review. Polish.

PMID:
19517854
6.

Genetic obesity syndromes.

Goldstone AP, Beales PL.

Front Horm Res. 2008;36:37-60. doi: 10.1159/0000115336. Review.

PMID:
18230893
7.

Specific genetic disorders and autism: clinical contribution towards their identification.

Cohen D, Pichard N, Tordjman S, Baumann C, Burglen L, Excoffier E, Lazar G, Mazet P, Pinquier C, Verloes A, Héron D.

J Autism Dev Disord. 2005 Feb;35(1):103-16. Review.

PMID:
15796126
8.

Cataracts associated with systemic disorders and syndromes.

Negahban K, Chern K.

Curr Opin Ophthalmol. 2002 Dec;13(6):419-22. Review.

PMID:
12441847
9.

[Cohen syndrome].

Kayashima T, Niikawa N.

Ryoikibetsu Shokogun Shirizu. 2001;(36):477-8. Review. Japanese. No abstract available.

PMID:
11596442
10.

Cohen syndrome: essential features, natural history, and heterogeneity.

Kivitie-Kallio S, Norio R.

Am J Med Genet. 2001 Aug 1;102(2):125-35. Review.

PMID:
11477603
11.

[Cohen syndrome].

Naritomi K.

Ryoikibetsu Shokogun Shirizu. 2001;(33):473-4. Review. Japanese. No abstract available.

PMID:
11462522
12.

[Cohen syndrome].

Kondo I.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):10-1. Review. Japanese. No abstract available.

PMID:
11057125
13.

[Cohen's syndrome: non-causal association with vascular rings].

Pérez-Caballero Macarrón C, Lozano Giménez C, Quintana Castilla A, Aparicio Meix JM.

An Esp Pediatr. 2000 Mar;52(3):289-95. Review. Spanish.

PMID:
11003912
14.

Cohen syndrome: evaluation of its cardiac, endocrine and radiological features.

Kivitie-Kallio S, Eronen M, Lipsanen-Nyman M, Marttinen E, Norio R.

Clin Genet. 1999 Jul;56(1):41-50. Review.

PMID:
10466416
15.

Prader-Willi and other syndromes associated with obesity and mental retardation.

Gunay-Aygun M, Cassidy SB, Nicholls RD.

Behav Genet. 1997 Jul;27(4):307-24. Review.

PMID:
9519559
16.

[Cohen syndrome. A new case and review of the literature].

Calzolari S, Ballardini M, De Marco P.

Minerva Pediatr. 1995 Mar;47(3):83-7. Review. Italian.

PMID:
7791717
17.

[Cohen syndrome. Personal case report and literature review].

Oztürk B, Weber HP.

Monatsschr Kinderheilkd. 1991 Dec;139(12):844-8. Review. German.

PMID:
1770962
18.

Tapetoretinal degeneration in brothers with apparent Cohen syndrome: nosology with Mirhosseini-Holmes-Walton syndrome.

Steinlein O, Tariverdian G, Boll HU, Vogel F.

Am J Med Genet. 1991 Nov 1;41(2):196-200. Review.

PMID:
1785634
19.

The Cohen syndrome: does mottled retina separate a Finnish and a Jewish type?

Kondo I, Nagataki S, Miyagi N.

Am J Med Genet. 1990 Sep;37(1):109-13. Review.

PMID:
2240027
20.

[Cohen syndrome. Description of a new case and study of the central nervous system using nuclear magnetic resonance].

Gabrielli O, Pierleoni C, Barbato M, Bonifazi V, Oggiano N, Carlucci A.

Minerva Pediatr. 1989 Dec;41(12):615-8. Review. Italian.

PMID:
2699519
Items per page

Supplemental Content

Loading ...
Write to the Help Desk