249 related articles for article (PubMed ID: 25327923)
21. Kindler syndrome.
Kaviarasan PK; Prasad PV; Shradda ; Viswanathan P
Indian J Dermatol Venereol Leprol; 2005; 71(5):348-50. PubMed ID: 16394462
[TBL] [Abstract][Full Text] [Related]
22. Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy.
Vahidnezhad H; Youssefian L; Saeidian AH; Mahmoudi H; Touati A; Abiri M; Kajbafzadeh AM; Aristodemou S; Liu L; McGrath JA; Ertel A; Londin E; Kariminejad A; Zeinali S; Fortina P; Uitto J
Matrix Biol; 2018 Mar; 66():22-33. PubMed ID: 29138120
[TBL] [Abstract][Full Text] [Related]
23. Kindler's Syndrome: A Tale of Two Siblings.
Handa N; Kachhawa D; Jain VK; Rao P; Das A
Indian J Dermatol; 2016; 61(4):468. PubMed ID: 27512212
[TBL] [Abstract][Full Text] [Related]
24. A Novel Nonsense Mutation in Exon 5 of KIND1 Gene in an Iranian Family with Kindler Syndrome.
Heidari MM; Khatami M; Kargar S; Azari M; Hoseinzadeh H; Fallah H
Arch Iran Med; 2016 Jun; 19(6):403-8. PubMed ID: 27293055
[TBL] [Abstract][Full Text] [Related]
25. Kindler surprise: mutations in a novel actin-associated protein cause Kindler syndrome.
White SJ; McLean WH
J Dermatol Sci; 2005 Jun; 38(3):169-75. PubMed ID: 15927810
[TBL] [Abstract][Full Text] [Related]
26. Acral skin atrophy in an infant: an early clue to Kindler syndrome diagnosis.
Diociaiuti A; Zambruno G; Giancristoforo S; Proto V; Boldrini R; Castiglia D; El Hachem M
J Eur Acad Dermatol Venereol; 2016 Jun; 30(6):1046-9. PubMed ID: 25764106
[No Abstract] [Full Text] [Related]
27. Expression of exon-8-skipped kindlin-1 does not compensate for defects of Kindler syndrome.
Natsuga K; Nishie W; Shinkuma S; Nakamura H; Matsushima Y; Tatsuta A; Komine M; Shimizu H
J Dermatol Sci; 2011 Jan; 61(1):38-44. PubMed ID: 21146372
[TBL] [Abstract][Full Text] [Related]
28. A novel mutation in the FERMT1 gene in Turkish siblings with Kindler syndrome.
Kartal D; Borlu M; Has C; Fölster-Holst R
J Eur Acad Dermatol Venereol; 2016 Jul; 30(7):1233-5. PubMed ID: 25865288
[No Abstract] [Full Text] [Related]
29. Kindler's syndrome. Report of a case.
Bordas X; Palou J; Capdevila JM; Mascaro JM
J Am Acad Dermatol; 1982 Feb; 6(2):263-5. PubMed ID: 7061748
[No Abstract] [Full Text] [Related]
30. [Corneal lesions in Kindler syndrome: a case report].
Chéour M; Mazlout H; Ben Jalel W; Brour J; Baroudi B; Kraiem A
J Fr Ophtalmol; 2012 Jan; 35(1):46.e1-5. PubMed ID: 21683471
[TBL] [Abstract][Full Text] [Related]
31. Kindler syndrome. Clinical and ultrastructural findings.
Haber RM; Hanna WM
Arch Dermatol; 1996 Dec; 132(12):1487-90. PubMed ID: 8961879
[TBL] [Abstract][Full Text] [Related]
32. Kindler syndrome in two related Kurdish families.
Hacham-Zadeh S; Garfunkel AA
Am J Med Genet; 1985 Jan; 20(1):43-8. PubMed ID: 3970073
[TBL] [Abstract][Full Text] [Related]
33. Kindler syndrome.
Ashton GH
Clin Exp Dermatol; 2004 Mar; 29(2):116-21. PubMed ID: 14987263
[TBL] [Abstract][Full Text] [Related]
34. Oxidative stress and mitochondrial dysfunction in Kindler syndrome.
Zapatero-Solana E; García-Giménez JL; Guerrero-Aspizua S; García M; Toll A; Baselga E; Durán-Moreno M; Markovic J; García-Verdugo JM; Conti CJ; Has C; Larcher F; Pallardó FV; Del Rio M
Orphanet J Rare Dis; 2014 Dec; 9():211. PubMed ID: 25528446
[TBL] [Abstract][Full Text] [Related]
35. Breast cancer in a patient with Kindlers syndrome.
Mehdi I; Al Bahrani BJ; Al Lawati TM; Mandhari ZA; Al Lawati FR
J Pak Med Assoc; 2017 Aug; 67(8):1283-1286. PubMed ID: 28839322
[TBL] [Abstract][Full Text] [Related]
36. Founder mutation c.676insC in three unrelated Kindler syndrome families belonging to a particular clan from Pakistan.
Shaiq PA; Klausegger A; Muzaffar F; Bauer JW; Khan MI; Khanum A; Qamar R; Raja GK
J Dermatol; 2012 Jul; 39(7):640-1. PubMed ID: 22220914
[No Abstract] [Full Text] [Related]
37. Kindler syndrome: the case of two Iranian sisters.
Kargar S; Shiryazdi SM; Neamatzadeh H; Ramazani V
G Ital Dermatol Venereol; 2018 Feb; 153(1):111-114. PubMed ID: 27391311
[TBL] [Abstract][Full Text] [Related]
38. Kindler's Syndrome with Recurrent Neutropenia: Report of Two Cases from Saudi Arabia.
Binamer Y; Chisti MA
J Pediatr Genet; 2023 Mar; 12(1):69-72. PubMed ID: 36684545
[TBL] [Abstract][Full Text] [Related]
39. A novel pathogenic FERMT1 variant in four families with Kindler syndrome in Argentina.
Valinotto LE; Natale MI; Lusso SB; Cella E; Gutiérrez O; Sebastiani F; Manzur GB
Pediatr Dermatol; 2020 Mar; 37(2):337-341. PubMed ID: 31957900
[TBL] [Abstract][Full Text] [Related]
40. Kindler's syndrome.
Alper JC; Baden HP; Goldsmith LA
Arch Dermatol; 1978 Mar; 114(3):457. PubMed ID: 629586
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
