106 related articles for article (PubMed ID: 4024679)
1. [Simultaneous occurrence of metageria and Gottron's acrogeria in one family].
Kaufmann I; Thiele B; Mahrle G
Z Hautkr; 1985 Jun; 60(12):975-84. PubMed ID: 4024679
[TBL] [Abstract][Full Text] [Related]
2. [Grotton's acrogeria with bone involvement].
Diepgen TL; Simon M
Hautarzt; 1990 Oct; 41(10):574-7. PubMed ID: 2258301
[TBL] [Abstract][Full Text] [Related]
3. [The Gottron syndrome from the dentist's viewpoint, case report].
Günther HM; Sitzmann F
Dtsch Zahnarztl Z; 1978 Dec; 33(12):873-5. PubMed ID: 282134
[TBL] [Abstract][Full Text] [Related]
4. [Association of a pediatric bullous eruption, cutaneous and muscular atrophy, hyperpigmentation and dysmorphism. A new entity?].
Sciolla JP; Guillot B; Barnéon G; Montoya P; Guilhou JJ; Meynadier J
Ann Dermatol Venereol; 1986; 113(4):317-27. PubMed ID: 3767229
[TBL] [Abstract][Full Text] [Related]
5. Generalized mottled pigmentation with postnatal skin blistering in three generations.
Westerhof W; Dingemans KP
J Am Acad Dermatol; 2004 May; 50(5 Suppl):S65-9. PubMed ID: 15097931
[TBL] [Abstract][Full Text] [Related]
6. Study of a family with a new progeroid syndrome.
Welsh O
Birth Defects Orig Artic Ser; 1975; 11(5):25-38. PubMed ID: 1240776
[TBL] [Abstract][Full Text] [Related]
7. [Gottron's acrogeria].
Raffi A; Laurent R; Agache P
Bull Soc Fr Dermatol Syphiligr; 1972; 79(1):34-7. PubMed ID: 4641735
[No Abstract] [Full Text] [Related]
8. Acrogeria (Gottron type): a vascular disorder?
Hashimoto C; Abe M; Onozawa N; Yokoyama Y; Ishikawa O
Br J Dermatol; 2004 Aug; 151(2):497-501. PubMed ID: 15327562
[TBL] [Abstract][Full Text] [Related]
9. [Gottron's acrogeria].
Cernohorský J; Rejf M; Zelnícek L; Rejfová M
Cesk Dermatol; 1975 Apr; 50(2):140-4. PubMed ID: 1139660
[No Abstract] [Full Text] [Related]
10. Gottron's acrogeria and sarcoidosis.
Meurer A; Lohmöller G; Keller C
Clin Investig; 1993 May; 71(5):387-91. PubMed ID: 8508010
[TBL] [Abstract][Full Text] [Related]
11. Hereditary Gottron's acrogeria with recessive transmission: a report of four cases in one family.
Rezai-Delui H; Lotfi N; Mamoori G; Rahimi MB
Pediatr Radiol; 1999 Feb; 29(2):124-30. PubMed ID: 9933333
[TBL] [Abstract][Full Text] [Related]
12. New progeroid disorder.
Penttinen M; Niemi KM; Vinkka-Puhakka H; Johansson R; Aula P
Am J Med Genet; 1997 Mar; 69(2):182-7. PubMed ID: 9056558
[TBL] [Abstract][Full Text] [Related]
13. [Hutchinson-Gilford syndrome].
Wollina U; Reuter A; Schaarschmidt H; Müller E; Maak B; Schmidt U
Hautarzt; 1992 Jul; 43(7):453-7. PubMed ID: 1506207
[TBL] [Abstract][Full Text] [Related]
14. [Combination in the one patient of acrogeria and Pasini--Pierini's idiopathic atrophoderma].
Krasnov BI; Kamenetskiĭ IS
Vestn Dermatol Venerol; 1973 Nov; 47(11):79-81. PubMed ID: 4779401
[No Abstract] [Full Text] [Related]
15. Cytogenetic investigations on Werner's syndrome, Acrogeria and Keratosis Palmo-Plantaris.
Elli R; Petrinelli P; Caporossi D; Nicoletti B; Antonelli A
J Genet Hum; 1983 Sep; 31(3):211-21. PubMed ID: 6228640
[TBL] [Abstract][Full Text] [Related]
16. [Gottron's acrogeria].
Bazyka AP
Vestn Dermatol Venerol; 1979 Feb; (2):31-6. PubMed ID: 425684
[No Abstract] [Full Text] [Related]
17. [The myxoma syndrome: "cardiac myxoma, cutaneous pigmented lesions and peripheral and endocrine neoplasms". Apropos 2 cases].
Zabala Argüelles JI; Maroto Alvaro E; Maroto Monedero C; García Fernández EJ; Mínguez García R; Vallés Serrano P; Moreno Belzué C; Arcas Meca R
Rev Esp Cardiol; 1994 Feb; 47(2):113-5. PubMed ID: 8165346
[TBL] [Abstract][Full Text] [Related]
18. GAPO syndrome in three relatives in a Turkish kindred.
Sayli BS; Gül D
Am J Med Genet; 1993 Sep; 47(3):342-5. PubMed ID: 8135278
[TBL] [Abstract][Full Text] [Related]
19. Kindler syndrome: report of three cases in a family and a brief review.
Yazdanfar A; Hashemi B
Int J Dermatol; 2009 Feb; 48(2):145-9. PubMed ID: 19200189
[TBL] [Abstract][Full Text] [Related]
20. Koraxitrachitic syndrome: a syndromic form of self-healing collodion baby with residual dappled atrophy of the derma.
Verloes A; Hermanns-Lê T; Lesenfants S; Lombet J; Lamotte PJ; Crèvecoeur-Liégeois C; Duchesne B; Piérard GE
Am J Med Genet; 1999 Oct; 86(5):454-8. PubMed ID: 10508988
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
