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Results: 19

Related Articles by Review for PubMed (Select 8062442)

1.

Multiple coagulation defects and the Cohen syndrome.

Schlichtemeier TL, Tomlinson GE, Kamen BA, Waber LJ, Wilson GN.

Clin Genet. 1994 Apr;45(4):212-6.

PMID:
8062442
2.

X-linked mental retardation with marfanoid habitus.

Fryns JP, Buttiens M.

Am J Med Genet. 1987 Oct;28(2):267-74. Review.

PMID:
3322000
3.

9q34.3 deletion syndrome in three unrelated children.

Iwakoshi M, Okamoto N, Harada N, Nakamura T, Yamamori S, Fujita H, Niikawa N, Matsumoto N.

Am J Med Genet A. 2004 Apr 30;126A(3):278-83. Review.

PMID:
15054842
4.

[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
5.

Cerebrovascular complications in cancer patients.

Rogers LR.

Neurol Clin. 2003 Feb;21(1):167-92. Review.

PMID:
12690649
6.

Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus).

Van Buggenhout G, Fryns JP.

Orphanet J Rare Dis. 2006 Jul 10;1:26. Review.

7.

Microcephaly, characteristic facies, joint abnormalities, and deficient leucocyte chemotaxis: a further case of the syndrome of Say et al.

Perandones C, Cerretini RI, Vargas Vera RM, Aranda EI, Alba LG, Pivetta OH.

J Med Genet. 1996 Mar;33(3):227-9. Review.

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11.

Haematologic disorders and cerebral venous thrombosis.

Akhtar N, Deleu D, Kamran S.

J Pak Med Assoc. 2006 Nov;56(11):498-501. Review.

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13.

Filippi syndrome: report of three additional cases.

Williams MS, Williams JL, Wargowski DS, Pauli RM, Pletcher BA.

Am J Med Genet. 1999 Nov 19;87(2):128-33. Review.

PMID:
10533026
14.

[Thyroid crisis and protein C deficiency in a case of superior sagittal sinus thrombosis].

Nagumo K, Fukushima T, Takahashi H, Sakakibara Y, Kojima S, Akikusa B.

Brain Nerve. 2007 Mar;59(3):271-6. Review. Japanese.

PMID:
17370653
15.

Nijmegen breakage syndrome.

van der Burgt I, Chrzanowska KH, Smeets D, Weemaes C.

J Med Genet. 1996 Feb;33(2):153-6. Review.

16.

[Cerebral sinus thrombosis in a patient with protein S deficiency: a case report].

Fujita A, Kuwamura K, Saitoh M, Sakagami Y, Takaishi Y, Suzuki S, Matsuo T, Tamaki N.

No Shinkei Geka. 1997 May;25(5):467-72. Review. Japanese.

PMID:
9145407
17.

[Familial Marfan's syndrome. A critical review and presentation of a clinical case].

Iannello S, Spina M, Prestipino M, Strano AM, Bellassai M, Politi G, Belfiore F.

Minerva Med. 1996 May;87(5):217-35. Review. Italian.

PMID:
8700348
18.

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
19.

[A case of marfanoid body habitus associated with an excessive hyperextensibility of the skin--an unclassified case in inherited connective tissue diseases].

Sakatsume Y, Saito M, Hara Y, Maruno Y, Sato K, Ishii J, Saito N, Hashimoto H, Saito K, Shinkai H.

Nihon Naika Gakkai Zasshi. 1988 Apr;77(4):499-505. Review. Japanese. No abstract available.

PMID:
3042899
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