受强制性开放获取政策约束的文章 - Lisa Weibel了解详情
无法在其他位置公开访问的文章：3 篇
Reduction of disease burden with early sirolimus treatment in a child with proteus syndrome
L Weibel, M Theiler, R Gnannt, K Neuhaus, JS Han, H Huber, ...
JAMA dermatology 157 (12), 1514-1516, 2021
强制性开放获取政策： US National Institutes of Health
Expanding the clinical spectrum of mosaic BRAF skin phenotypes
A Sorlin, V Carmignac, J Amiel, O Boccara, S Fraitag, A Maruani, ...
Journal of the European Academy of Dermatology and Venereology 35 (10), e690 …, 2021
强制性开放获取政策： National Institute of Health and Medical Research, France, Agence Nationale …
PTCH1 inactivation is sufficient to cause basaloid follicular hamartoma in paediatric Nevoid basal cell carcinoma syndrome.
G Blanchard, AA Yurchenko, OT Pop, L Weibel, M Theiler, V Hauser, ...
Journal of the European Academy of Dermatology & Venereology 36 (11), 2022
强制性开放获取政策： Swiss National Science Foundation, Swiss Cancer Foundation
可在其他位置公开访问的文章：13 篇
Integrin α3 Mutations with Kidney, Lung, and Skin Disease
C Has, G Spartà, D Kiritsi, L Weibel, A Moeller, V Vega-Warner, A Waters, ...
New England Journal of Medicine 366 (16), 1508-1514, 2012
强制性开放获取政策： US National Institutes of Health
Germline loss-of-function mutations in EPHB4 cause a second form of capillary malformation-arteriovenous malformation (CM-AVM2) deregulating RAS-MAPK signaling
M Amyere, N Revencu, R Helaers, E Pairet, E Baselga, M Cordisco, ...
Circulation 136 (11), 1037-1048, 2017
强制性开放获取政策： US National Institutes of Health, National Fund for Scientific Research, Belgium
Mutations in three genes encoding proteins involved in hair shaft formation cause uncombable hair syndrome
FBÜ Basmanav, L Cau, A Tafazzoli, MC Méchin, S Wolf, MT Romano, ...
The American Journal of Human Genetics 99 (6), 1292-1304, 2016
强制性开放获取政策： German Research Foundation, National Institute of Health and Medical …
Secukinumab therapy for Netherton syndrome
I Luchsinger, N Knöpfel, M Theiler, MB Des Claustres, C Barbieux, ...
JAMA dermatology 156 (8), 907-911, 2020
强制性开放获取政策： Agence Nationale de la Recherche
Differential expression of secreted factors SOSTDC1 and ADAMTS8 cause profibrotic changes in linear morphoea fibroblasts
II Badshah, S Brown, L Weibel, A Rose, B Way, N Sebire, G Inman, ...
British Journal of Dermatology 180 (5), 1135-1149, 2019
强制性开放获取政策： Cancer Research UK, National Institute for Health Research, UK
Assessment of the genetic spectrum of uncombable hair syndrome in a cohort of 107 individuals
FB Basmanav, N Cesarato, S Kumar, O Borisov, P Kokordelis, DJ Ralser, ...
JAMA dermatology 158 (11), 1245-1253, 2022
强制性开放获取政策： German Research Foundation, Federal Ministry of Education and Research, Germany
Life-threatening primary varicella zoster virus infection with hemophagocytic lymphohistiocytosis-like disease in GATA2 haploinsufficiency accompanied by expansion of double …
S Prader, M Felber, B Volkmer, J Trück, A Schwieger-Briel, M Theiler, ...
Frontiers in immunology 9, 2766, 2018
强制性开放获取政策： Wellcome Trust
Sleep behavior of infants with infantile hemangioma treated with propranolol—a cohort study
M Theiler, N Knöpfel, S von der Heydt, A Schwieger-Briel, I Luchsinger, ...
European Journal of Pediatrics 180 (8), 2655-2668, 2021
强制性开放获取政策： Swiss National Science Foundation
The cause of follicular spicules in multiple myeloma
GA Hosler, L Weibel, RC Wang
JAMA dermatology 151 (4), 457-458, 2015
强制性开放获取政策： US National Institutes of Health
Molecular characterization and natural history of linear porokeratosis: A case series
M Saleva-Stateva, M Hess, K Technau-Hafsi, L Weibel, MA Badea, ...
Journal of the American Academy of Dermatology 85 (6), 1603-1606, 2021
强制性开放获取政策： German Research Foundation, Federal Ministry of Education and Research, Germany
Dermatological signs lead to discovery of mosaic ACTB variants in segmental odontomaxillary dysplasia
S Polubothu, D Abdin, M Barysch, A Thomas, N Bulstrode, R Evans, ...
British Journal of Dermatology 183 (6), 1128-1130, 2020
强制性开放获取政策： National Institute for Health Research, UK, Wellcome Trust
Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss
N Cesarato, A Schwieger-Briel, Y Gossmann, SK Henne, K Hillmann, ...
British Journal of Dermatology 189 (6), 741-749, 2023
强制性开放获取政策： German Research Foundation, Federal Ministry of Education and Research, Germany
Three novel pathogenic NEK9 variants in patients with nevus comedonicus: A case series
HA Juratli, S Jägle, M Theiler, D Didona, R Happle, N Knöpfel, L Weibel, ...
Journal of the American Academy of Dermatology 86 (4), 958-960, 2022
强制性开放获取政策： German Research Foundation
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