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Poikiloderma of Kindler
Known as:
POIKILODERMA, HEREDITARY ACROKERATOTIC
, Poikiloderma, congenital, with bullae, weary type
, KNDLRS
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National Institutes of Health
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Related topics
Related topics
10 relations
Autosomal recessive inheritance
Dental caries
FERMT1, 1-BP INS, 1714A
Grooving of nail
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Broader (4)
Bulla
Epidermolysis Bullosa
Periodontal Diseases
Photosensitivity Disorders
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Genotypic Heterogeneity and the Mode of Inheritance in Epidermolysis Bullosa.
J. Uitto
,
H. Vahidnezhad
,
L. Youssefian
JAMA dermatology
2016
Corpus ID: 4018304
Epidermolysis bullosa (EB) comprises a clinically heterogeneousgroupofdisorderscharacterizedbyfragilityof skin, leading to…
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2014
2014
Kindler syndrome in mice and men
Elizabeth K Duperret
,
T. Ridky
Cancer Biology & Therapy
2014
Corpus ID: 28901456
Kindler syndrome (KS) in humans is a severe skin blistering disease associated with inflammation and increased risk of epidermal…
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2011
2011
A Case of Poikiloderma Vasculare Atrophicans
M. Choi
,
J. Lee
,
Seong-Jin Kim
,
Seung-Chul Lee
,
Y. Won
,
S. Yun
Annals of Dermatology
2011
Corpus ID: 15925549
Poikiloderma vasculare atrophicans (PVA) is a rare variant of mycosis fungoides, and is characterized by generalized…
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2008
2008
Kindler syndrome: a study of five Egyptian cases with evaluation of severity
E. Nofal
,
M. Assaf
,
Khaled Elmosalamy
International Journal of Dermatology
2008
Corpus ID: 23693787
Background Kindler syndrome (KS) is a rare genodermatosis characterized by four major features (acral blisters, photosensitivity…
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2007
2007
A microwave-assisted synthesis of julolidine-9-carboxamide derivatives and their conversion to chalcogenoxanthones via directed metalation.
Jason J. Holt
,
Brandon D. Calitree
,
Josiah Vincek
,
M. K. Gannon
,
M. Detty
Journal of Organic Chemistry
2007
Corpus ID: 1603224
9-formyljulolidine was oxidized via a microwave-assisted Willgerodt-Kindler reaction to the N-piperidine or N-morpholine…
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2006
2006
Retrospective diagnosis of Kindler syndrome in a 37‐year‐old man
M. Thomson
,
G. Ashton
,
J. Mcgrath
,
R. Eady
,
C. Moss
Clincal and Experimental Dermatology
2006
Corpus ID: 6342243
Kindler syndrome is a rare autosomal recessive disorder characterized by acral blisters in infancy and early childhood, followed…
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2004
2004
Gene symbol: Kind1. Disease: kindler syndrome.
C. Lanschuetzer
,
W. Muss
,
+4 authors
H. Hintner
Human Genetics
2004
Corpus ID: 8431950
2002
2002
Kongenitale bullöse Poikilodermie (Kindler-Syndrom)
B. Binder
,
D. Metze
,
J. Smolle
Der Hautarzt
2002
Corpus ID: 34389962
ZusammenfassungEs wird über eine 18-jährige Patientin berichtet, die wegen Synechien der Labien zur weiteren Abklärung überwiesen…
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1998
1998
Poikiloderma‐like Cutaneous Amyloidosis in an Ethnic Chinese Girl
M. Ho
,
L. Chong
Journal of dermatology (Print)
1998
Corpus ID: 26083262
Primary cutaneous amyloidosis is the deposition of amyloid in the skin without involvement of internal organs. It is easily…
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1994
1994
Release of acquired syndactylies in Kindler syndrome.
S. Szczerba
,
K. Yokoo
,
B. Bauer
Annals of Plastic Surgery
1994
Corpus ID: 43098676
Kindler syndrome is a rare, blistering skin disease characterized by acral bullae, poikiloderma, and diffuse cutaneous atrophy…
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