Hausser, I.
136  results:
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1

Quality of life and clinical characteristics of self‐improv..:

Hake, L. ; Süßmuth, K. ; Komlosi, K....
Journal of the European Academy of Dermatology and Venereology.  36 (2022)  4 - p. 582-591 , 2022
 
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2

Diagnosis of Ehlers–Danlos syndrome: data deficiency still ..:

Hausser, I.
British Journal of Dermatology.  182 (2019)  3 - p. 535-536 , 2019
 
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3

Identification of mutations in SDR9C7 in six families with ..:

Hotz, A. ; Fagerberg, C. ; Vahlquist, A....
British Journal of Dermatology.  178 (2018)  3 - p. e207-e209 , 2018
 
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4

Acral lamellar Ichthyosis – expanding the phenotype of temp..:

de Almeida Jr, H. ; Has, C. ; Fischer, J..
Journal of the European Academy of Dermatology and Venereology.  32 (2017)  5 - p. , 2017
 
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5

Ichthyoses: new insights unravel defects in skin barrier fu..:

Hausser, I.
British Journal of Dermatology.  176 (2017)  4 - p. 863-864 , 2017
 
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6

Sixteen novel mutations in PNPLA1 in patients with autosoma..:

Zimmer, A.D. ; Kim, G.J. ; Hotz, A....
British Journal of Dermatology.  177 (2017)  2 - p. 445-455 , 2017
 
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7

At first sight or second glance: clinical presentation of m..:

Toberer, F. ; Happle, R. ; Schneiderbauer, R....
Journal of the European Academy of Dermatology and Venereology.  31 (2017)  11 - p. 1912-1915 , 2017
 
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8

Association of Cole disease with novel heterozygous mutatio..:

Schlipf, N.A. ; Traupe, H. ; Gilaberte, Y....
British Journal of Dermatology.  174 (2016)  5 - p. 1152-1156 , 2016
 
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9

Two novel mutations in the LOR gene in three families with ..:

Hotz, A. ; Bourrat, E. ; Hausser, I....
British Journal of Dermatology.  172 (2015)  4 - p. 1158-1162 , 2015
 
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10

Ehlers-Danlos-like-Syndrom bei einer Katze:

Weingart, C. ; Haußer, I. ; Kershaw, O..
Schweizer Archiv für Tierheilkunde.  156 (2014)  11 - p. 543-548 , 2014
 
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11

Loss of desmoglein 1 associated with palmoplantar keratoder..:

Has, C. ; Jakob, T. ; He, Y....
British Journal of Dermatology.  172 (2014)  1 - p. 257-261 , 2014
 
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12

A mouse organotypic tissue culture model for autosomal rece..:

Rosenberger, S. ; Dick, A. ; Latzko, S....
British Journal of Dermatology.  171 (2014)  6 - p. 1347-1357 , 2014
 
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13

Novel mutation in theCLDN1gene in a Turkish family with neo..:

Kirchmeier, P. ; Sayar, E. ; Hotz, A....
British Journal of Dermatology.  170 (2014)  4 - p. 976-978 , 2014
 
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14

Phenotypic spectrum of epidermolysis bullosa associated wit..:

Schumann, H. ; Kiritsi, D. ; Pigors, M....
British Journal of Dermatology.  169 (2013)  1 - p. 115-124 , 2013
 
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15

Complete filaggrin deficiency in ichthyosis vulgaris is ass..:

Perusquía‐Ortiz, A.M. ; Oji, V. ; Sauerland, M.C....
Journal of the European Academy of Dermatology and Venereology.  27 (2013)  12 - p. 1552-1558 , 2013
 
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