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Items: 1 to 20 of 93

1.

Ruvalcaba-Myhre-Smith syndrome: a case with probable autosomal-dominant inheritance and additional manifestations.

DiLiberti JH, Weleber RG, Budden S.

Am J Med Genet. 1983 Jul;15(3):491-5.

PMID:
6881215
2.

Ruvalcaba-Myhre-Smith syndrome.

Gretzula JC, Hevia O, Schachner LS, DiLiberti JH, Ruvalcaba RH, Schimschock JR, Weleber RG, Halal F, Lipson MH, Blumberg B, et al.

Pediatr Dermatol. 1988 Feb;5(1):28-32.

PMID:
3380760
3.

A new lipid storage myopathy observed in individuals with the Ruvalcaba-Myhre-Smith syndrome.

DiLiberti JH, D'Agostino AN, Ruvalcaba RH, Schimschock JR.

Am J Med Genet. 1984 May;18(1):163-7.

PMID:
6741991
4.

Sotos syndrome with intestinal polyposis and pigmentary changes of the genitalia.

Ruvalcaba RH, Myhre S, Smith DW.

Clin Genet. 1980 Dec;18(6):413-6.

PMID:
7449178
5.
6.

[Ruvalcaba-Myhre-Smith syndrome].

Nakahara A, Kashimura H.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):68-70. Review. Japanese. No abstract available.

PMID:
11057146
7.

Clinicopathologic findings in the Bannayan-Riley-Ruvalcaba syndrome.

Fargnoli MC, Orlow SJ, Semel-Concepcion J, Bolognia JL.

Arch Dermatol. 1996 Oct;132(10):1214-8.

PMID:
8859033
8.

Adenomatous changes in the hamartomatous polyps of Ruvalcaba-Myhre-Smith syndrome.

Coyle WJ, Ryan MT, Nowicki MJ.

J Clin Gastroenterol. 1998 Jan;26(1):85-7. No abstract available.

PMID:
9492874
9.

What syndrome is this? Ruvalcaba-Myhre-Smith syndrome.

Bishop PR, Nowicki MJ, Parker PH.

Pediatr Dermatol. 2000 Jul-Aug;17(4):319-21. No abstract available.

PMID:
10990586
10.

Heredofamilial syndrome of mesodermal hamartomas, macrocephaly, and pseudopapilledema.

Dvir M, Beer S, Aladjem M.

Pediatrics. 1988 Feb;81(2):287-90.

PMID:
3340479
11.
12.
13.

Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage.

Charrow J, Listernick R, Ward K.

Am J Med Genet. 1993 Mar 1;45(5):606-8.

PMID:
8456833
15.

Duodenojejunal intussusception secondary to hamartomatous polyps of duodenum surrounding the ampulla of Vater.

Hwang CS, Chu CC, Chen KC, Chen A.

J Pediatr Surg. 2001 Jul;36(7):1073-5.

PMID:
11431783
16.

Cole-Hughes macrocephaly syndrome and associated autistic manifestations.

Naqvi S, Cole T, Graham JM Jr.

Am J Med Genet. 2000 Sep 11;94(2):149-52.

PMID:
10982971
17.

Cronkhite Canada syndrome: report of a case with spontaneous recovery.

Viranuvatti V, Damrongsak C, Chainuvati T, Vanasin B, Chandrcharoensin C.

J Med Assoc Thai. 1981 May;64(5):261-6. No abstract available.

PMID:
7252395
18.

Inherited macrocephaly-hamartoma syndromes.

DiLiberti JH.

Am J Med Genet. 1998 Oct 2;79(4):284-90. Review.

PMID:
9781909
19.

Peutz-Jeghers syndrome: is family screening needed?

Baumgartner G, Neuweiler J, Herzog D.

Pediatr Surg Int. 2000;16(5-6):437-9.

PMID:
10955585
20.

Café au lait spots in ataxia-telangiectasia (A.T.). Histochemical and ultrastructural study in one case.

Ortonne JP, Claudy AL, Freycon F.

Arch Dermatol Res. 1980;268(1):91-9.

PMID:
7416802

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