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Results: 1 to 20 of 33

Related Articles by Review for PubMed (Select 10826616)

1.

Radial aplasia, poikiloderma and auto-immune enterocolitis--new syndrome or severe form of Rothmund-Thomson syndrome?

Hilhorst-Hofstee Y, Shah N, Atherton D, Harper JI, Milla P, Winter RM.

Clin Dysmorphol. 2000 Apr;9(2):79-85.

PMID:
10826616
2.

[Rothmund syndrome or Thomson syndrome. An analysis of the literature exemplified by a personal case].

Vanscheidt E, Wolff G, Niederhoff H, Greiner P.

Monatsschr Kinderheilkd. 1988 May;136(5):264-9. Review. German.

PMID:
3043208
3.

Rothmund-Thomson syndrome: a report of two patients and a review of the literature.

Moss C.

Br J Dermatol. 1990 Jun;122(6):821-9. Review.

PMID:
2196075
4.

Rothmund-Thomson syndrome: review of the world literature.

Vennos EM, Collins M, James WD.

J Am Acad Dermatol. 1992 Nov;27(5 Pt 1):750-62. Review.

PMID:
1430398
5.

Meier-Gorlin syndrome: report of eight additional cases and review.

Bongers EM, Opitz JM, Fryer A, Sarda P, Hennekam RC, Hall BD, Superneau DW, Harbison M, Poss A, van Bokhoven H, Hamel BC, Knoers NV.

Am J Med Genet. 2001 Aug 1;102(2):115-24. Review.

PMID:
11477602
6.

An unusual patient with Rothmund-Thomson syndrome, porokeratosis and bilateral iris dysgenesis.

Mak RK, Griffiths WA, Mellerio JE.

Clin Exp Dermatol. 2006 May;31(3):401-3. Review.

PMID:
16681588
7.

[Congenital poikiloderma].

Marghescu S.

Z Hautkr. 1989 Mar 15;64(3):167-9. Review. German.

PMID:
2655322
8.

Poikiloderma congenitale: case report and review of the literature.

Collins P, Barnes L, McCabe M.

Pediatr Dermatol. 1991 Mar;8(1):58-60. Review.

PMID:
1862027
9.

Rothmund-Thomson syndrome with osteosarcoma.

Drouin CA, Mongrain E, Sasseville D, Bouchard HL, Drouin M.

J Am Acad Dermatol. 1993 Feb;28(2 Pt 2):301-5. Review.

PMID:
8436644
10.

Rothmund-Thomson syndrome.

Vennos EM, James WD.

Dermatol Clin. 1995 Jan;13(1):143-50. Review.

PMID:
7712640
11.

[Congenital poikilodermas].

Rodermund OE.

Z Hautkr. 1988 Oct 15;63(10):866-8. Review. German.

PMID:
3070992
12.

Congenital poikiloderma with unusual hypopigmentation and acral blistering at birth.

Ogunbiyi AO, Ogunbiyi JO, Baiyeroju-Agbeja AM.

J Eur Acad Dermatol Venereol. 1999 Jan;12(1):54-8. Review.

PMID:
10188152
13.

The cerebro-costo-mandibular syndrome: seven patients and review of the literature.

van den Ende JJ, Schrander-Stumpel C, Rupprecht E, Meinecke P, Maroteaux P, de Die-Smulders C, Hamel BC.

Clin Dysmorphol. 1998 Apr;7(2):87-95. Review.

PMID:
9571277
14.

Hereditary bullous acrokeratotic poikiloderma of Weary-Kindler associated with pseudoainhum and sclerotic bands.

Krunic AL, Medenica L, Novak A, Carlos G, Clark RE.

Int J Dermatol. 1997 Jul;36(7):529-33. Review. No abstract available. Erratum in: Int J Dermatol. 2007 Apr;46(4):446. Ljiljana, M [corrected to Medenica, L].

PMID:
9268754
15.

Poikiloderma with neutropenia: a case report and review of the literature.

Farruggia P, Indaco S, Dufour C, Lanza T, Mosa C, Macaluso A, Milioto M, D'Angelo P, Lanciotti M.

J Pediatr Hematol Oncol. 2014 May;36(4):297-300. doi: 10.1097/MPH.0b013e31829f35e7. Review.

PMID:
23823120
16.

Expanding the phenotypic spectrum of the Baller-Gerold syndrome.

Temtamy SA, Aglan MS, Nemat A, Eid M.

Genet Couns. 2003;14(3):299-312. Review.

PMID:
14577674
17.

Kindler syndrome: report of a case with ultrastructural study and review of the literature.

Patrizi A, Pauluzzi P, Neri I, Trevisan G, De Giorgi LB, Pasquinelli G.

Pediatr Dermatol. 1996 Sep-Oct;13(5):397-402. Review.

PMID:
8893241
18.

Radial longitudinal deficiency.

Maschke SD, Seitz W, Lawton J.

J Am Acad Orthop Surg. 2007 Jan;15(1):41-52. Review.

PMID:
17213381
19.

Short root anomaly associated with Rothmund-Thomson syndrome.

Roinioti TD, Stefanopoulos PK.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007 Jan;103(1):e19-22. Epub 2006 Oct 24. Review.

PMID:
17178481
20.

[Congenital amegakaryocytic thrombopenia with radial aplasia].

Corberand J, Dutau G, Delsol G, Rochiccioli P.

Ann Pediatr (Paris). 1976 Jan 2;23(1):73-8. Review. French. No abstract available.

PMID:
16104254
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