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Results: 1 to 20 of 121

1.

New progeroid disorder.

Penttinen M, Niemi KM, Vinkka-Puhakka H, Johansson R, Aula P.

Am J Med Genet. 1997 Mar 17;69(2):182-7.

PMID:
9056558
[PubMed - indexed for MEDLINE]
2.

Transient progeroid phenotype and lipodystrophy in mosaic polyploidy.

Kárteszi J, Kosztolányi G, Czakó M, Hadzsiev K, Morava E.

Clin Dysmorphol. 2006 Jan;15(1):29-31.

PMID:
16317304
[PubMed - indexed for MEDLINE]
3.

Skeletal abnormalities of acrogeria, a progeroid syndrome.

Ho A, White SJ, Rasmussen JE.

Skeletal Radiol. 1987;16(6):463-8.

PMID:
3659993
[PubMed - indexed for MEDLINE]
4.

Lethal neonatal Hutchinson-Gilford progeria syndrome.

Rodríguez JI, Pérez-Alonso P, Funes R, Pérez-Rodríguez J.

Am J Med Genet. 1999 Jan 29;82(3):242-8.

PMID:
10215548
[PubMed - indexed for MEDLINE]
5.

Acro-osteolysis, keloid like-lesions, distinctive facial features, and overgrowth: two newly recognized patients with premature aging syndrome, Penttinen type.

Zufferey F, Hadj-Rabia S, De Sandre-Giovannoli A, Dufier JL, Leheup B, Schweitze C, Bodemer C, Cormier-Daire V, Le Merrer M.

Am J Med Genet A. 2013 Jul;161A(7):1786-91. doi: 10.1002/ajmg.a.35984. Epub 2013 May 29.

PMID:
23720404
[PubMed - indexed for MEDLINE]
6.

Hutchinson-Gilford progeria syndrome: review of the phenotype.

Hennekam RC.

Am J Med Genet A. 2006 Dec 1;140(23):2603-24. Review.

PMID:
16838330
[PubMed - indexed for MEDLINE]
7.

Natural course of neonatal progeroid syndrome.

Hou JW.

Pediatr Neonatol. 2009 Jun;50(3):102-9. doi: 10.1016/S1875-9572(09)60044-9.

PMID:
19579756
[PubMed - indexed for MEDLINE]
8.

Juvenile hyaline fibromatosis.

Larralde M, Santos-Muñoz A, Calb I, Magariños C.

Pediatr Dermatol. 2001 Sep-Oct;18(5):400-2.

PMID:
11737684
[PubMed - indexed for MEDLINE]
9.

Premature aging syndrome with osteosarcoma, cataracts, diabetes mellitus, osteoporosis, erythroid macrocytosis, severe growth and developmental deficiency.

Okamoto N, Satomura K, Hatsukawa Y, Hayashida M, Saijo K, Ohno T, Goto M.

Am J Med Genet. 1997 Mar 17;69(2):169-70.

PMID:
9056555
[PubMed - indexed for MEDLINE]
10.

A maternally transmitted lethal neonatal progeroid syndrome with prominent genitourinary and gastrointestinal features.

Delatycki MB, Cleary MA, Bankier A, McDougall PN, Ahluwalia JS, Chow CW, Cooke-Yarborough CM.

J Med Genet. 1997 Jun;34(6):520-4.

PMID:
9192279
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Petty-Laxova-Wiedemann progeroid syndrome: further phenotypical delineation and confirmation of a rare syndrome of premature aging.

Delgado-Luengo WN, Petty EM, Solís-Añez E, Römel O, Delgado-Luengo J, Hernández ML, Morales-Machín A, Borjas-Fuentes L, Zabala-Fernández W, González-Ferrer S, Pineda-Bernal L, Pardo-Govea T, Martínez-Basalo MC, González R, Urdaneta K, Cañizales J, Fleitas-Cabello H.

Am J Med Genet A. 2009 Oct;149A(10):2200-5. doi: 10.1002/ajmg.a.32884.

PMID:
19725131
[PubMed - indexed for MEDLINE]
12.

[Juvenile hyaline fibromatosis].

Haddad J, Dandach A, Gebran S, Rhayel L, Aftimos G.

Arch Pediatr. 1997 Dec;4(12):1200-3. French.

PMID:
9538423
[PubMed - indexed for MEDLINE]
13.

Mulvihill-Smith progeria-like syndrome: a further report with delineation of phenotype, immunologic deficits, and novel observation of fibroblast abnormalities.

de Silva DC, Wheatley DN, Herriot R, Brown T, Stevenson DA, Helms P, Dean JC.

Am J Med Genet. 1997 Mar 3;69(1):56-64. Review.

PMID:
9066884
[PubMed - indexed for MEDLINE]
14.

Wiedemann-Rautenstrauch neonatal progeroid syndrome: report of three new patients.

Arboleda H, Quintero L, Yunis E.

J Med Genet. 1997 May;34(5):433-7.

PMID:
9152846
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

The De Barsy syndrome.

Guerra D, Fornieri C, Bacchelli B, Lugli L, Torelli P, Balli F, Ferrari P.

J Cutan Pathol. 2004 Oct;31(9):616-24.

PMID:
15330994
[PubMed - indexed for MEDLINE]
16.

Lethal progeroid syndrome with osteolysis. Case report.

Le Merrer M, Guillot M, Briard ML, Maroteaux P.

Ann Genet. 1991;34(2):82-4.

PMID:
1746888
[PubMed - indexed for MEDLINE]
17.

Atypical progeroid syndrome: an unknown helicase gene defect?

Ruijs MW, van Andel RN, Oshima J, Madan K, Nieuwint AW, Aalfs CM.

Am J Med Genet A. 2003 Jan 30;116A(3):295-9.

PMID:
12503110
[PubMed - indexed for MEDLINE]
18.

The Wiedemann-Rautenstrauch neonatal progeroid syndrome: a case report and review of the literature.

Bitoun P, Lachassine E, Sellier N, Sauvion S, Gaudelus J.

Clin Dysmorphol. 1995 Jul;4(3):239-45.

PMID:
7551161
[PubMed - indexed for MEDLINE]
19.

Mandibuloacral dysplasia: a rare progeroid syndrome. Two brothers confirm autosomal recessive inheritance.

Pallotta R, Morgese G.

Clin Genet. 1984 Aug;26(2):133-8.

PMID:
6467666
[PubMed - indexed for MEDLINE]
20.

Neonatal progeroid syndrome: more than one disease?

Hagadorn JI, Wilson WG, Hogge WA, Callicott JH, Beale EF.

Am J Med Genet. 1990 Jan;35(1):91-4.

PMID:
2301475
[PubMed - indexed for MEDLINE]

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