232 related articles for article (PubMed ID: 11230626)
1. Café au lait spots: the pediatrician's perspective.
Tekin M; Bodurtha JN; Riccardi VM
Pediatr Rev; 2001 Mar; 22(3):82-90. PubMed ID: 11230626
[No Abstract] [Full Text] [Related]
2. Café-au-lait Macules and Neurofibromatosis Type 1: A Review of the Literature.
Bernier A; Larbrisseau A; Perreault S
Pediatr Neurol; 2016 Jul; 60():24-29.e1. PubMed ID: 27212418
[TBL] [Abstract][Full Text] [Related]
3. Café au lait spots: When and how to pursue their genetic origins.
Lalor L; Davies OMT; Basel D; Siegel DH
Clin Dermatol; 2020; 38(4):421-431. PubMed ID: 32972601
[TBL] [Abstract][Full Text] [Related]
4. [Brown spots on the whole body: the mother has them as well. Neurofibromatosis].
Stiefelhagen P
MMW Fortschr Med; 2013 Nov; 155 Spec No 2():7, 35. PubMed ID: 24734438
[No Abstract] [Full Text] [Related]
5. The diagnostic and clinical significance of café-au-lait macules.
Shah KN
Pediatr Clin North Am; 2010 Oct; 57(5):1131-53. PubMed ID: 20888463
[TBL] [Abstract][Full Text] [Related]
6. Halolike Phenomenon Around a Café au Lait Spot Superimposed on a Mongolian Spot.
Neri I; Lambertini M; Tengattini V; Rivalta B; Patrizi A
Pediatr Dermatol; 2017 May; 34(3):e152-e153. PubMed ID: 28523880
[TBL] [Abstract][Full Text] [Related]
7. Diagnostic outcome in children with multiple café au lait spots.
Korf BR
Pediatrics; 1992 Dec; 90(6):924-7. PubMed ID: 1344978
[TBL] [Abstract][Full Text] [Related]
8. Café-au-lait spots.
Cohen JB; Janniger CK; Schwartz RA
Cutis; 2000 Jul; 66(1):22-4. PubMed ID: 10916686
[No Abstract] [Full Text] [Related]
9. [Café-au-lait spots].
Lacour JP
Ann Dermatol Venereol; 1999 Oct; 126(10):749-54. PubMed ID: 10604023
[No Abstract] [Full Text] [Related]
10. The great mimicker: Phenotypic overlap between constitutional mismatch repair deficiency and Tuberous Sclerosis complex.
Shapira Rootman M; Goldberg Y; Cohen R; Kropach N; Keidar I; Friedland R; Dotan G; Konen O; Toledano H
Clin Genet; 2020 Feb; 97(2):296-304. PubMed ID: 31730237
[TBL] [Abstract][Full Text] [Related]
11. Multiple café au lait spots in familial patients with MAP2K2 mutation.
Takenouchi T; Shimizu A; Torii C; Kosaki R; Takahashi T; Saya H; Kosaki K
Am J Med Genet A; 2014 Feb; 164A(2):392-6. PubMed ID: 24311457
[TBL] [Abstract][Full Text] [Related]
12. [Neurofibromatosis type 1--own experiences].
Czajkowski G; Kałuzny J; Jatczak-Gaca A; Wysocki M
Klin Oczna; 2010; 112(1-3):45-8. PubMed ID: 20572503
[TBL] [Abstract][Full Text] [Related]
13. Multiple café au lait macules and Crowe sign.
López Aventín D; Gilaberte M; Pujol RM
Arch Dermatol; 2011 Jun; 147(6):735-40. PubMed ID: 21690543
[No Abstract] [Full Text] [Related]
14. Multiple or familial café-au-lait spots is neurofibromatosis type 6: clarification of a diagnosis.
Madson JG
Dermatol Online J; 2012 May; 18(5):4. PubMed ID: 22630574
[TBL] [Abstract][Full Text] [Related]
15. [Skin manifestations of Fanconi anemia].
Ogilvie P; Hofmann UB; Bröcker EB; Hamm H
Hautarzt; 2002 Apr; 53(4):253-7. PubMed ID: 12053693
[TBL] [Abstract][Full Text] [Related]
16. Congenital Pigmentary Anomalies in the Newborn.
Habeshian KA; Kirkorian AY
Neoreviews; 2021 Oct; 22(10):e660-e672. PubMed ID: 34599064
[TBL] [Abstract][Full Text] [Related]
17. Café-au-lait spots in schoolchildren.
Burwell RG; James NJ; Johnston DI
Arch Dis Child; 1982 Aug; 57(8):631-2. PubMed ID: 6810767
[TBL] [Abstract][Full Text] [Related]
18. Clinical aspects of neurofibromatosis 1.
North KN
Eur J Paediatr Neurol; 1998; 2(5):223-31. PubMed ID: 10726824
[No Abstract] [Full Text] [Related]
19. Radiology case of the month. Café-au-lait spots. Neurofibromatosis type 1.
Gupta A; Neitzschman HR; Schroder M
J La State Med Soc; 2002; 154(5):221-2. PubMed ID: 12440746
[No Abstract] [Full Text] [Related]
20. Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage.
Charrow J; Listernick R; Ward K
Am J Med Genet; 1993 Mar; 45(5):606-8. PubMed ID: 8456833
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
