159 related articles for article (PubMed ID: 36932209)
1. [Update on nevi and nevoid skin disorders].
Happle R
Dermatologie (Heidelb); 2023 May; 74(5):310-315. PubMed ID: 36932209
[TBL] [Abstract][Full Text] [Related]
2. Cutis marmorata telangiectatica congenita being caused by postzygotic GNA11 mutations.
Schuart C; Bassi A; Kapp F; Wieland I; Pagliazzi A; Losch H; Mazzatenta C; Bacci GM; Oranges T; Schanze D; Mohnike K; Nanda A; Fischer J; Zenker M; Happle R
Eur J Med Genet; 2022 May; 65(5):104472. PubMed ID: 35351629
[TBL] [Abstract][Full Text] [Related]
3. What is a capillary malformation?
Happle R
J Am Acad Dermatol; 2008 Dec; 59(6):1077-9. PubMed ID: 19022106
[TBL] [Abstract][Full Text] [Related]
4. Born in the Purple: An Exceptional Case of Cutis Marmorata Telangiectatica Congenita.
Kyriakou G; Gialeli E; Vryzaki E; Georgiou S
Acta Dermatovenerol Croat; 2020 Dec; 28(4):247-248. PubMed ID: 33835001
[TBL] [Abstract][Full Text] [Related]
5. The case of a boy with nevus of Ota, extensive Mongolian spot, nevus flammeus, nevus anemicus and cutis marmorata telangiectatica congenita: a unique instance of phacomatosis pigmentovascularis.
Ma H; Liao M; Qiu S; Luo R; Lu R; Lu C
An Bras Dermatol; 2015; 90(3 Suppl 1):10-2. PubMed ID: 26312661
[TBL] [Abstract][Full Text] [Related]
6. [Syndromes with vascular skin anomalies].
Happle R
Hautarzt; 2019 Jul; 70(7):474-480. PubMed ID: 31111168
[TBL] [Abstract][Full Text] [Related]
7. Cutis marmorata telangiectatica congenita: a case report.
Altman AR; Tschen JA; Wolf JE
Pediatr Dermatol; 1984 Jan; 1(3):223-5. PubMed ID: 6494067
[TBL] [Abstract][Full Text] [Related]
8. Cerebriform sebaceous nevus: a subtype of organoid nevus due to specific postzygotic FGFR2 mutations.
Theiler M; Weibel L; Christen-Zaech S; Carmignac V; Sorlin A; Neuhaus K; Chevarin M; Thauvin-Robinet C; Philippe C; Faivre L; Vabres P; Kuentz P
J Eur Acad Dermatol Venereol; 2021 Oct; 35(10):2085-2090. PubMed ID: 33930231
[TBL] [Abstract][Full Text] [Related]
9. Cutis marmorata telangiectatica congenita manifesting as port-wine stain at birth.
Imafuku S; Tashiro A; Furue M; Nakayama J
J Dermatol; 2008 Jul; 35(7):471-2. PubMed ID: 18705838
[No Abstract] [Full Text] [Related]
10. Cutis marmorata telangiectatica congenita: report of 22 cases.
Picascia DD; Esterly NB
J Am Acad Dermatol; 1989 Jun; 20(6):1098-1104. PubMed ID: 2666459
[TBL] [Abstract][Full Text] [Related]
11. Cutis marmorata telangiectatica congenita with cerebral and ophthalmic anomalies: report of one case.
Mu SC; Hung HY; Chiu NC; Chen HH; Chen LJ
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(1):65-8. PubMed ID: 9066194
[TBL] [Abstract][Full Text] [Related]
12. Cutis marmorata telangiectatica congenita: clinicopathologic characteristics and differential diagnosis.
Cohen PR; Zalar GL
Cutis; 1988 Dec; 42(6):518-22. PubMed ID: 3229141
[TBL] [Abstract][Full Text] [Related]
13. [Bilateral congenital glaucoma in a child with cutis marmorata telangiectatica congenita: a case report].
Spitzer MS; Szurman P; Rohrbach JM; Aisenbrey S
Klin Monbl Augenheilkd; 2007 Jan; 224(1):66-9. PubMed ID: 17260324
[TBL] [Abstract][Full Text] [Related]
14. Congenital glaucoma associated with cutis marmorata telangiectatica congenita: two case reports.
Sato SE; Herschler J; Lynch PJ; Hodes BL; Fryczkowski AW; Schlosser HD
J Pediatr Ophthalmol Strabismus; 1988; 25(1):13-7. PubMed ID: 3343635
[TBL] [Abstract][Full Text] [Related]
15. Dohi Memorial Lecture. New aspects of cutaneous mosaicism.
Happle R
J Dermatol; 2002 Nov; 29(11):681-92. PubMed ID: 12484429
[TBL] [Abstract][Full Text] [Related]
16. Mosaic pathogenic variants in AKT3 cause capillary malformation and undergrowth.
Bolli A; Nriagu B; Britt AD; Toole AD; Treat J; Srinivasan A; Sheppard SE
Am J Med Genet A; 2023 May; 191(5):1442-1446. PubMed ID: 36695285
[TBL] [Abstract][Full Text] [Related]
17. Ocular findings in cutis marmorata telangiectatica congenita. Bilateral exudative vitreoretinopathy.
Pendergast SD; Trese MT; Shastry BS
Retina; 1997; 17(4):306-9. PubMed ID: 9279946
[TBL] [Abstract][Full Text] [Related]
18. Vascular Stains: Proposal for a Clinical Classification to Improve Diagnosis and Management.
Rozas-Muñoz E; Frieden IJ; Roé E; Puig L; Baselga E
Pediatr Dermatol; 2016 Nov; 33(6):570-584. PubMed ID: 27456075
[TBL] [Abstract][Full Text] [Related]
19. A case of phakomatosis pigmentovascularis type II: port-wine stain and dermal melanocytosis with cutis marmorata telangiectatica congenita-like lesions.
Namiki T; Arai M; Miura K; Yokozeki H
Eur J Dermatol; 2016 Jun; 26(3):302-3. PubMed ID: 26905386
[No Abstract] [Full Text] [Related]
20. Unusual case of phakomatosis pigmentovascularis in a Japanese female infant associated with three phakomatoses: Port-wine stain, dermal melanocytosis and cutis marmorata telangiectatica congenita.
Shimizu N; Nakagawa K; Taguchi M; Okabayashi A; Kishida M; Kinoshita R; Imanishi H; Fukai K; Tsuruta D
J Dermatol; 2015 Oct; 42(10):1006-7. PubMed ID: 26104843
[No Abstract] [Full Text] [Related]
[Next] [New Search]