Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 105

1.

Cantu syndrome and lymphoedema.

García-Cruz D, Mampel A, Echeverria MI, Vargas AL, Castañeda-Cisneros G, Davalos-Rodriguez N, Patiño-Garcia B, Garcia-Cruz MO, Castañeda V, Cardona EG, Marin-Solis B, Cantu JM, Nuñez-Reveles N, Moran-Moguel C, Thavanati PK, Ramirez-Garcia S, Sanchez-Corona J.

Clin Dysmorphol. 2011 Jan;20(1):32-7. doi: 10.1097/MCD.0b013e32833d015c.

PMID:
20890180
[PubMed - indexed for MEDLINE]
2.

Pulmonary hypertension secondary to partial pulmonary venous obstruction in a child with Cantu syndrome.

Kobayashi D, Cook AL, Williams DA.

Pediatr Pulmonol. 2010 Jul;45(7):727-9. doi: 10.1002/ppul.21215.

PMID:
20575102
[PubMed - indexed for MEDLINE]
3.

Cantú syndrome: report of nine new cases and expansion of the clinical phenotype.

Scurr I, Wilson L, Lees M, Robertson S, Kirk E, Turner A, Morton J, Kidd A, Shashi V, Stanley C, Berry M, Irvine AD, Goudie D, Turner C, Brewer C, Smithson S.

Am J Med Genet A. 2011 Mar;155A(3):508-18. doi: 10.1002/ajmg.a.33885. Epub 2011 Feb 22.

PMID:
21344641
[PubMed - indexed for MEDLINE]
4.

Three patients with the osteochondrodysplasia and hypertrichosis syndrome--Cantu syndrome.

Rosser EM, Kaariainen H, Hurst JA, Baraitser M, Hall CM, Clayton P, Leonard JV.

Clin Dysmorphol. 1998 Apr;7(2):79-85. Review.

PMID:
9571276
[PubMed - indexed for MEDLINE]
5.

A familial case of Cantu craniofaciofronto digital syndrome.

Garcia-Gonzalez CL, Garcia-Cruz D, Garcia-Cruz MO, Castañeda-Cisneros G, Garcia-Ortiz JE, Orozco-Gutiérrez MH, Sanchez-Corona J.

Clin Dysmorphol. 2012 Jul;21(3):162-6. doi: 10.1097/MCD.0b013e328353a082. No abstract available.

PMID:
22504422
[PubMed - indexed for MEDLINE]
6.

Cantu syndrome in a woman and her two daughters: Further confirmation of autosomal dominant inheritance and review of the cardiac manifestations.

Grange DK, Lorch SM, Cole PL, Singh GK.

Am J Med Genet A. 2006 Aug 1;140(15):1673-80.

PMID:
16835932
[PubMed - indexed for MEDLINE]
7.

Congenital hypertrichosis, cardiomegaly and mild osteochondrodysplasia.

Nevin NC, Mulholland HC, Thomas PS.

Am J Med Genet. 1996 Dec 2;66(1):33-8.

PMID:
8957508
[PubMed - indexed for MEDLINE]
8.

Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Cantú syndrome.

Robertson SP, Kirk E, Bernier F, Brereton J, Turner A, Bankier A.

Am J Med Genet. 1999 Aug 6;85(4):395-402.

PMID:
10398267
[PubMed - indexed for MEDLINE]
9.

Lymphoedema in hereditary recurrent cholestasis from birth.

Aagenaes O, Sigstad H, Bjorn-Hansen R.

Arch Dis Child. 1970 Oct;45(243):690-5. No abstract available.

PMID:
5477684
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Congenital hypertrichosis, cardiomegaly, and osteochondrodysplasia (Cantú syndrome): a new case with unusual radiological findings.

Concolino D, Formicola S, Camera G, Strisciuglio P.

Am J Med Genet. 2000 May 29;92(3):191-4.

PMID:
10817653
[PubMed - indexed for MEDLINE]
11.

Interstitial magnetic resonance lymphography: the clinical effectiveness of a new method.

Dimakakos E, Koureas A, Koutoulidis V, Skiadas V, Katsenis K, Arkadopoulos N, Gouliamos A, Vlachos L.

Lymphology. 2008 Sep;41(3):116-25.

PMID:
19013879
[PubMed - indexed for MEDLINE]
12.

Lymphatic abnormalities in Noonan's syndrome.

Lanning P, Similä S, Suramo I, Paavilainen T.

Pediatr Radiol. 1978 Jun 19;7(2):106-9.

PMID:
673526
[PubMed - indexed for MEDLINE]
13.

[Primary lymphedema in the nephrotic syndrome: case report].

Wagner U, Balzar E, Khoss A, Partsch H.

Wien Klin Wochenschr. 1987 Sep 25;99(18):652-5. German.

PMID:
3687024
[PubMed - indexed for MEDLINE]
14.

Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.

Engels H, Bosse K, Ehrbrecht A, Zahn S, Hoischen A, Propping P, Bindl L, Reutter H.

Am J Med Genet. 2002 Aug 1;111(2):205-9. Review.

PMID:
12210352
[PubMed - indexed for MEDLINE]
15.

Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly).

Lazalde B, Sánchez-Urbina R, Nuño-Arana I, Bitar WE, de Lourdes Ramírez-Dueñas M.

Am J Med Genet. 2000 Oct 23;94(5):421-7. Review.

PMID:
11050630
[PubMed - indexed for MEDLINE]
16.

The dermal lymphatics in lymphoedema visualized by indirect lymphography.

Partsch H, Urbanek A, Wenzel-Hora B.

Br J Dermatol. 1984 Apr;110(4):431-8.

PMID:
6712887
[PubMed - indexed for MEDLINE]
17.

Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24.

Brice G, Mansour S, Bell R, Collin JR, Child AH, Brady AF, Sarfarazi M, Burnand KG, Jeffery S, Mortimer P, Murday VA.

J Med Genet. 2002 Jul;39(7):478-83.

PMID:
12114478
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Lymphoedema due to lymphatic hyperplasia: a case report.

Rasooly R, Haskell L, Haskell Y.

Radiogr Today. 1989 Jun;55(625):30.

PMID:
2590438
[PubMed - indexed for MEDLINE]
19.

Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: further delineation of a new genetic syndrome.

Garcia-Cruz D, Sánchez-Corona J, Nazará Z, Garcia-Crúz MO, Figuera LE, Castañeda V, Cantú JM.

Am J Med Genet. 1997 Mar 17;69(2):138-51.

PMID:
9056550
[PubMed - indexed for MEDLINE]
20.

Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities - support for the role of K(ATP) channels in this condition.

Brownstein CA, Towne MC, Luquette LJ, Harris DJ, Marinakis NS, Meinecke P, Kutsche K, Campeau PM, Yu TW, Margulies DM, Agrawal PB, Beggs AH.

Eur J Med Genet. 2013 Dec;56(12):678-82. doi: 10.1016/j.ejmg.2013.09.009. Epub 2013 Oct 28.

PMID:
24176758
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk