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Results: 1 to 20 of 210

1.

Familial variable expression of dilated cardiomyopathy in Alström syndrome: a report of four sibs.

Hoffman JD, Jacobson Z, Young TL, Marshall JD, Kaplan P.

Am J Med Genet A. 2005 May 15;135(1):96-8.

PMID:
15809999
[PubMed - indexed for MEDLINE]
2.

A rare cause of dilated cardiomyopathy; Alström syndrome.

Unlü C, Ustün I, Akay F, Doğan U.

Anadolu Kardiyol Derg. 2008 Aug;8(4):316-7. No abstract available.

PMID:
18676317
[PubMed - indexed for MEDLINE]
Free Article
3.

Three new cases of Alström syndrome.

Benso C, Hadjadj E, Conrath J, Denis D.

Graefes Arch Clin Exp Ophthalmol. 2002 Aug;240(8):622-7. Epub 2002 Jul 20.

PMID:
12192455
[PubMed - indexed for MEDLINE]
4.

Alström syndrome and cecal volvulus in 2 siblings.

Khoo EY, Risley J, Zaitoun AM, El-Sheikh M, Paisey RB, Acheson AG, Mansell P.

Am J Med Sci. 2009 May;337(5):383-5. doi: 10.1097/MAJ.0b013e3181926594.

PMID:
19440062
[PubMed - indexed for MEDLINE]
5.

The Alström syndrome: is it a rare or unknown disease?

Maffei P, Munno V, Marshall JD, Scandellari C, Sicolo N.

Ann Ital Med Int. 2002 Oct-Dec;17(4):221-8. Review.

PMID:
12532560
[PubMed - indexed for MEDLINE]
6.

A rare case of Alström syndrome presenting with rapidly progressive severe dilated cardiomyopathy diagnosed by echocardiography.

Makaryus AN, Popowski B, Kort S, Paris Y, Mangion J.

J Am Soc Echocardiogr. 2003 Feb;16(2):194-6.

PMID:
12574750
[PubMed - indexed for MEDLINE]
7.

Molecular analysis and long-term clinical evaluation of three siblings with Alström syndrome.

Ozgül RK, Satman I, Collin GB, Hinman EG, Marshall JD, Kocaman O, Tütüncü Y, Yilmaz T, Naggert JK.

Clin Genet. 2007 Oct;72(4):351-6.

PMID:
17850632
[PubMed - indexed for MEDLINE]
8.

Homozygosity mapping at Alström syndrome to chromosome 2p.

Collin GB, Marshall JD, Cardon LR, Nishina PM.

Hum Mol Genet. 1997 Feb;6(2):213-9.

PMID:
9063741
[PubMed - indexed for MEDLINE]
Free Article
9.

Natural history of Alström syndrome in early childhood: onset with dilated cardiomyopathy.

Michaud JL, Héon E, Guilbert F, Weill J, Puech B, Benson L, Smallhorn JF, Shuman CT, Buncic JR, Levin AV, Weksberg R, Brevière GM.

J Pediatr. 1996 Feb;128(2):225-9.

PMID:
8636816
[PubMed - indexed for MEDLINE]
10.

Alström syndrome.

Marshall JD, Beck S, Maffei P, Naggert JK.

Eur J Hum Genet. 2007 Dec;15(12):1193-202. Epub 2007 Oct 17.

PMID:
17940554
[PubMed - indexed for MEDLINE]
Free Article
11.

[Alström syndrome: clinical and genetic features, and a diagnostic guide to foresee complications].

Mendioroz J, Bermejo E, Marshall JD, Naggert JK, Collin GB, Martínez-Frías ML.

Med Clin (Barc). 2008 Nov 29;131(19):741-6. Spanish.

PMID:
19091203
[PubMed - indexed for MEDLINE]
12.

Alstrom syndrome in four sibs from northern Jordan.

Hamamy H, Barham M, Alkhawaldeh AE, Cockburn D, Snowden H, Ajlouni K.

Ann Saudi Med. 2006 Nov-Dec;26(6):480-3. No abstract available.

PMID:
17146208
[PubMed - indexed for MEDLINE]
13.

Cardiac manifestations of Alström syndrome: echocardiographic findings.

Makaryus AN, Zubrow ME, Marshall JD, Gillam LD, Mangion JR.

J Am Soc Echocardiogr. 2007 Dec;20(12):1359-63. Epub 2007 Sep 6.

PMID:
17825523
[PubMed - indexed for MEDLINE]
14.

New Alström syndrome phenotypes based on the evaluation of 182 cases.

Marshall JD, Bronson RT, Collin GB, Nordstrom AD, Maffei P, Paisey RB, Carey C, Macdermott S, Russell-Eggitt I, Shea SE, Davis J, Beck S, Shatirishvili G, Mihai CM, Hoeltzenbein M, Pozzan GB, Hopkinson I, Sicolo N, Naggert JK, Nishina PM.

Arch Intern Med. 2005 Mar 28;165(6):675-83.

PMID:
15795345
[PubMed - indexed for MEDLINE]
15.

Rare case of Alstrom syndrome with empty sella and interfamilial presence of Bardet-Biedl phenotype.

Catrinoiu D, Mihai CM, Tuta L, Stoicescu R, Simpetru A.

J Med Life. 2009 Jan-Mar;2(1):98-103.

PMID:
20108498
[PubMed - indexed for MEDLINE]
16.

Ophthalmologic and systemic features of the Alström syndrome: report of 9 cases.

Van den Abeele K, Craen M, Schuil J, Meire FM.

Bull Soc Belge Ophtalmol. 2001;(281):67-72.

PMID:
11702646
[PubMed - indexed for MEDLINE]
17.

Familial insulin resistant diabetes associated with acanthosis nigricans, polycystic ovaries, hypogonadism, pigmentary retinopathy, labyrinthine deafness, and mental retardation.

Boor R, Herwig J, Schrezenmeir J, Pontz BF, Schönberger W.

Am J Med Genet. 1993 Mar 1;45(5):649-53.

PMID:
8456839
[PubMed - indexed for MEDLINE]
18.

Alstrom syndrome: confirmation of linkage to chromosome 2p12-13 and phenotypic heterogeneity in three affected sibs.

Zumsteg U, Muller PY, Miserez AR.

J Med Genet. 2000 Jul;37(7):E8. No abstract available.

PMID:
10882760
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Evaluation of insulin resistant diabetes mellitus in Alström syndrome: a long-term prospective follow-up of three siblings.

Satman I, Yilmaz MT, Gürsoy N, Karşidağ K, Dinççağ N, Ovali T, Karadeniz S, Uysal V, Buğra Z, Okten A, Devrim S.

Diabetes Res Clin Pract. 2002 Jun;56(3):189-96.

PMID:
11947966
[PubMed - indexed for MEDLINE]
20.

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
[PubMed - indexed for MEDLINE]

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