183 related articles for article (PubMed ID: 27088932)
1. Phacomatosis pigmentovascularis: Report of four new cases.
Nanda A; Al-Abdulrazzaq HK; Habeeb YK; Zakkiriah M; Alghadhfan F; Al-Noun R; Al-Ajmi H
Indian J Dermatol Venereol Leprol; 2016; 82(3):298-303. PubMed ID: 27088932
[TBL] [Abstract][Full Text] [Related]
2. Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review.
Kumar A; Zastrow DB; Kravets EJ; Beleford D; Ruzhnikov MRZ; Grove ME; Dries AM; Kohler JN; Waggott DM; Yang Y; Huang Y; ; Mackenzie KM; Eng CM; Fisher PG; Ashley EA; Teng JM; Stevenson DA; Shieh JT; Wheeler MT; Bernstein JA
Am J Med Genet A; 2019 Jun; 179(6):966-977. PubMed ID: 30920161
[TBL] [Abstract][Full Text] [Related]
3. Phacomatosis cesiomarmorata with hypospadias and phacomatosis cesioflammea with Sturge-Weber syndrome, Klippel-Trenaunay syndrome and aplasia of veins -- case reports with rare associations.
Kaur T; Sharma N; Sethi A; Kooner S; Banger H
Dermatol Online J; 2015 Sep; 21(9):. PubMed ID: 26437284
[TBL] [Abstract][Full Text] [Related]
4. Red-white and blue baby: a case of phacomatosis pigmentovascularis type V.
Byrom L; Surjana D; Yoong C; Zappala T
Dermatol Online J; 2015 Jun; 21(6):. PubMed ID: 26158369
[TBL] [Abstract][Full Text] [Related]
5. Phacomatosis pigmentovascularis revisited and reclassified.
Happle R
Arch Dermatol; 2005 Mar; 141(3):385-8. PubMed ID: 15781681
[TBL] [Abstract][Full Text] [Related]
6. Phacomatosis spilorosea versus phacomatosis melanorosea: a critical reappraisal of the worldwide literature with updated classification of phacomatosis pigmentovascularis.
Torchia D
Acta Dermatovenerol Alp Pannonica Adriat; 2021 Mar; 30(1):27-30. PubMed ID: 33765754
[TBL] [Abstract][Full Text] [Related]
7. Phacomatosis melanorosea without extracutaneous features: an unusual type of phacomatosis pigmentovascularis.
Arnold AW; Kleine MU; Happle R
Eur J Dermatol; 2012; 22(4):473-5. PubMed ID: 22713702
[TBL] [Abstract][Full Text] [Related]
8. Phacomatosis pigmentovascularis with sturge-weber syndrome and congenital glaucoma: A rare case report.
Manavalan V; Kaliaperumal S; Subramanian S; Mani M
Eur J Ophthalmol; 2021 Dec; ():11206721211067886. PubMed ID: 34918572
[TBL] [Abstract][Full Text] [Related]
9. Phacomatosis pigmentovascularis type 2b (phacomatosis cesioflammea) with double superior vena cava, abdominal varicosities, and natal tooth: Novel associations.
Singal A; Mittal H; Aggarwal A; Das S; Manchanda S
Pediatr Dermatol; 2018 May; 35(3):e151-e154. PubMed ID: 29479730
[TBL] [Abstract][Full Text] [Related]
10. Phacomatosis pigmentovascularis of cesioflammea type in 7 patients: combination of ocular pigmentation (melanocytosis or melanosis) and nevus flammeus with risk for melanoma.
Shields CL; Kligman BE; Suriano M; Viloria V; Iturralde JC; Shields MV; Say EA; Shields JA
Arch Ophthalmol; 2011 Jun; 129(6):746-50. PubMed ID: 21670341
[TBL] [Abstract][Full Text] [Related]
11. Phacomatosis pigmentovascularis type Va in a 3-month old.
Larralde M; Santos-Muñoz A; Rodríguez Cáceres M; Ciardiullo A
Pediatr Dermatol; 2008; 25(2):198-200. PubMed ID: 18429779
[TBL] [Abstract][Full Text] [Related]
12. The risk of glaucoma associated with phacomatosis cesioflammea and phacomatosis cesioflammeo-marmorata.
Huang S; Yang Y; Ouyang Z; Guo X; Zhan Z; Liu X; Chen Z; Xu J; Yu M
Eur J Dermatol; 2022 Sep; 32(5):589-596. PubMed ID: 36468718
[TBL] [Abstract][Full Text] [Related]
13. Phacomatosis pigmentovascularis of cesioflammea type.
Villarreal DJ; Leal F
An Bras Dermatol; 2016; 91(5 suppl 1):54-56. PubMed ID: 28300894
[TBL] [Abstract][Full Text] [Related]
14. Large aberrant Mongolian spots coexisting with cutis marmorata telangiectatica congenita (phacomatosis pigmentovascularis type V or phacomatosis cesiomarmorata).
Torrelo A; Zambrano A; Happle R
J Eur Acad Dermatol Venereol; 2006 Mar; 20(3):308-10. PubMed ID: 16503893
[TBL] [Abstract][Full Text] [Related]
15. [Phakomatosis pigmentovascularis cesioflammea: a case report].
Viada Peláez MC; Stefano PC; Cirio A; Cervini AB
Arch Argent Pediatr; 2018 Feb; 116(1):e121-e124. PubMed ID: 29333836
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Phacomatosis pigmentovascularis type IIIb.
Seckin D; Yucelten D; Aytug A; Demirkesen C
Int J Dermatol; 2007 Sep; 46(9):960-3. PubMed ID: 17822502
[TBL] [Abstract][Full Text] [Related]
18. Phacomatosis pigmentovascularis type IIa--case report.
Segatto MM; Schmitt EU; Hagemann LN; Silva RC; Cattani CA
An Bras Dermatol; 2013; 88(6 Suppl 1):85-8. PubMed ID: 24346888
[TBL] [Abstract][Full Text] [Related]
19. Phacomatosis cesioflammea: first case report from India.
Goyal T; Varshney A
Indian J Dermatol Venereol Leprol; 2010; 76(3):307. PubMed ID: 20445318
[TBL] [Abstract][Full Text] [Related]
20. Phacomatosis cesioflammea with unilateral lipohypoplasia.
Castori M; Rinaldi R; Angelo C; Zambruno G; Grammatico P; Happle R
Am J Med Genet A; 2008 Feb; 146A(4):492-5. PubMed ID: 18203153
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
