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Results of search for 'su:"Epidermolysis Bullosa Simplex"', page 5 of 26
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Authors
Anton-Lamprecht, I
Bauer, Johann W
Bruckner-Tuderman, Leena
Coulombe, P A
Eady, R A
Fine, J D
Fuchs, E
Has, Cristina
Jonkman, M F
Jonkman, Marcel F
Lane, E B
Leigh, I M
Magin, Thomas M
Mellerio, J E
Rugg, E L
Sawamura, Daisuke
Shimizu, H
Sybert, V P
Uitto, J
Uitto, Jouni
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Adult
Child
Child, Preschool
Epidermolysis Bullosa Simplex
Female
Humans
Keratin-14
Keratin-5
Keratinocytes
Keratins
Male
Mutation
Pedigree
Phenotype
Skin
chemistry
complications
genetics
metabolism
pathology
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81.
Coexistence of KRT14 and KRT5 mutations in a Polish patient with epidermolysis bullosa simplex.
[electronic resource]
by
Wertheim-Tysarowska, K
Sota, J
Kutkowska-Kaźmierczak, A
Woźniak, K
Bal, J
Kowalewski, C
Producer:
20141114
In:
The British journal of dermatology
vol. 170
Online resources:
Available from publisher's website
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82.
Topical Diacerein Ointment for Epidermolysis Bullosa Simplex: A Review
[electronic resource]
by
Limmer, Allison L
Nwannunu, Crystal E
Shah, Radhika
Coleman, Kendall
Patel, Ravi R
Mui, Uyen Ngoc
Tyring, Stephen K
Producer:
20191209
In:
Skin therapy letter
vol. 24
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83.
Digenic inheritance of KRT5 and KRT14 mutations in a family with epidermolysis bullosa simplex.
[electronic resource]
by
Yu, Yueqian
Mi, Zihao
Fu, Xi'an
Wang, Zhenzhen
Sun, Lele
Liu, Hong
Zhang, Furen
Producer:
20210329
In:
The Australasian journal of dermatology
vol. 61
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84.
Epidermolysis bullosa of the Dowling-Meara type: clinical and ultrastructural findings in five patients.
[electronic resource]
by
Puddu, P
Angelo, C
Faraggiana, T
Onetti Muda, A
Colonna, L
Paradisi, M
Producer:
19961121
In:
Pediatric dermatology
vol. 13
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85.
Epidermolysis bullosa simplex Dowling-Meara: troublesome blistering and pruritus in an adult patient.
[electronic resource]
by
McGrath, J A
Burrows, N P
Russell Jones, R
Eady, R A
Producer:
19930325
In:
Dermatology (Basel, Switzerland)
vol. 186
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86.
Gene symbol: KRT14. Disease: Epidermolysis bullosa simplex.
[electronic resource]
by
Schneider, H
Muehle, C
Producer:
20051011
In:
Human genetics
vol. 117
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87.
Definitive radiotherapy for Merkel cell carcinoma in the setting of epidermolysis bullosa simplex.
[electronic resource]
by
Ong, Wee Loon
Bailey, Eliza
McCormack, Christopher
Weston, Lauren
Morgan, Vanessa
McDowell, Lachlan
Producer:
20191227
In:
The Australasian journal of dermatology
vol. 60
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88.
Immunohistochemical detection of keratin with the monoclonal antibody MNF116 is useful in the diagnosis of epidermolysis bullosa simplex.
[electronic resource]
by
Prieto, V G
McNutt, N S
Producer:
19940825
In:
Journal of cutaneous pathology
vol. 21
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89.
A new keratin 5 mutation (K199T) in a family with Weber-Cockayne epidermolysis bullosa simplex.
[electronic resource]
by
Xu, Z
Dong, H
Sun, X
Zhu, X
Yang, Y
Producer:
20040301
In:
Clinical and experimental dermatology
vol. 29
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90.
Ptosis and ophthalmoplegia associated with epidermolysis bullosa simplex-muscular dystrophy.
[electronic resource]
by
Auringer, David E
Simon, John W
Meyer, Dale R
Malone, Anthony
Producer:
20110304
In:
Ophthalmic plastic and reconstructive surgery
vol. 26
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91.
The many faces of plectin and plectinopathies: pathology and mechanisms.
[electronic resource]
by
Winter, Lilli
Wiche, Gerhard
Producer:
20130806
In:
Acta neuropathologica
vol. 125
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92.
Plectin mutations underlie epidermolysis bullosa simplex in 8% of patients.
[electronic resource]
by
Bolling, Marieke C
Jongbloed, Jan D H
Boven, Ludolf G
Diercks, Gilles F H
Smith, Frances J D
Irwin McLean, W H
Jonkman, Marcel F
Producer:
20140304
In:
The Journal of investigative dermatology
vol. 134
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93.
Genetic skin disorders of keratin.
[electronic resource]
by
Fuchs, E
Producer:
19930127
In:
The Journal of investigative dermatology
vol. 99
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94.
Inherited blistering diseases of the skin.
[electronic resource]
by
Fine, J D
Johnson, L B
Wright, J T
Producer:
19911217
In:
Pediatrician
vol. 18
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95.
Anterior corneal disease of epidermolysis bullosa simplex.
[electronic resource]
by
Adamis, A P
Schein, O D
Kenyon, K R
Producer:
19930510
In:
Archives of ophthalmology (Chicago, Ill. : 1960)
vol. 111
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96.
Keratotic lesions in epidermolysis bullosa simplex with mottled pigmentation.
[electronic resource]
by
Yasukawa, Kana
Sawamura, Daisuke
Akiyama, Masashi
Motoda, Natsuki
Shimizu, Hiroshi
Producer:
20050920
In:
Journal of the American Academy of Dermatology
vol. 52
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97.
Epidermolysis bullosa simplex with mottled pigmentation.
[electronic resource]
by
Browning, John C
Mohr, Brooke
Producer:
20120604
In:
Dermatology online journal
vol. 18
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98.
A novel homozygous deletion in EXPH5 causes a skin fragility phenotype.
[electronic resource]
by
Malchin, N
Sarig, O
Grafi-Cohen, M
Geller, S
Goldberg, I
Shani, A
Gat, A
Sprecher, E
Mashiah, J
Producer:
20180112
In:
Clinical and experimental dermatology
vol. 41
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99.
HLA and epidermolysis bullosa: evidence for independent assortment of Weber-Cockayne subtype of epidermolysis bullosa and HLA complex.
[electronic resource]
by
Vaidya, S
Tyring, S K
Feldkamp, M
Johnson, L B
Fine, J D
Producer:
19911001
In:
Journal of dermatological science
vol. 2
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100.
Kallin syndrome associated with vitiligo.
[electronic resource]
by
El Darouti, M A
El Hawary, M S
Abdel Hay, R M
Producer:
20150917
In:
Clinical and experimental dermatology
vol. 40
Online resources:
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