E Guenova
PTCH1 inactivation is sufficient to cause basaloid follicular hamartoma in paediatric Nevoid basal cell carcinoma syndrome.
Blanchard G, Yurchenko A, Pop O, Weibel L, Theiler M, Hauser V, Fraitag S, Guenova E, Flatz L, Nikolaev S, Hohl D. PTCH1 inactivation is sufficient to cause basaloid follicular hamartoma in paediatric Nevoid basal cell carcinoma syndrome. J Eur Acad Dermatol Venereol 2022; 36:e954-e956.
08.07.2022PTCH1 inactivation is sufficient to cause basaloid follicular hamartoma in paediatric Nevoid basal cell carcinoma syndrome.
08.07.2022J Eur Acad Dermatol Venereol 2022; 36:e954-e956
Blanchard G, Yurchenko A A, Pop O T, Weibel Lisa, Theiler M, Hauser V, Fraitag S, Guenova E, Flatz Lukas, Nikolaev S I, Hohl D
Multicentric EORTC retrospective study shows efficacy of brentuximab vedotin in patients who have mycosis fungoides and Sézary syndrome with variable CD30 positivity
Papadavid E, Bagot M, Hodak E, Guenova E, Guiron R, Dimitriou F, Cozzio A, Vico C, Ortiz-Romero P, Quaglino P, Engelina S, Porkert S, Jonak C, Dalamaga M, Iliakis T, Nikolaou V, Pappa V, Kapniari E, Scarisbrick J. Multicentric EORTC retrospective study shows efficacy of brentuximab vedotin in patients who have mycosis fungoides and Sézary syndrome with variable CD30 positivity. Br J Dermatol 2021; 185:1035-1044.
17.08.2021Multicentric EORTC retrospective study shows efficacy of brentuximab vedotin in patients who have mycosis fungoides and Sézary syndrome with variable CD30 positivity
17.08.2021Br J Dermatol 2021; 185:1035-1044
Papadavid E, Bagot M, Hodak E, Guenova E, Guiron R, Dimitriou F, Cozzio Antonio, Vico C, Ortiz-Romero P L, Quaglino P, Engelina S, Porkert S, Jonak C, Dalamaga M, Iliakis T, Nikolaou V, Pappa V, Kapniari E, Scarisbrick J
The PROCLIPI international registry of early-stage mycosis fungoides identifies substantial diagnostic delay in most patients
Yoo J, Busschots A, Hauben E, Bervoets A, Woei-A-Jin F, Matin R, Collins G, Weatherhead S, Frew J, Bayne M, Dunnill G, McKay P, Ranki A, Vakeva L, Vydianath B, Amel-Kashipaz R, Marinos L, Oikonomidi A, Stratigos A, Vignon-Pennamen M, Climent F, Gonzalez-Barca E, Georgiou E, Senetta R, Zinzani P, Arumainathan A, Azurdia R, Klemke C, Enz P, Pujol R, Quint K, Geskin L, Hong E, Evison F, Vermeer M, Cerroni L, Kempf W, Kim Y, Bur C, Folkes A, Benstead K, Twigger R, Rieger K, Brown R, Sanches J, Miyashiro D, Akilov O, McCann S, Sahi H, Damasco F, Querfeld C, Willemze R, Latzka J, Scarisbrick J, Whittaker S, Nikolaou V, Tomasini C, Amitay I, Prag Naveh H, Ram-Wolff C, Battistella M, Alberti-Violetti S, Stranzenbach R, Gargallo V, Muniesa C, Child F, Guenova E, Quaglino P, Prince H, Papadavid E, Hodak E, Bagot M, Servitje O, Berti E, Ortiz-Romero P, Stadler R, Patsatsi A, Knobler R, Koletsa T, Jonak C, Wobser M, Geissinger E, Wehkamp U, Weichenthal M, Cowan R, Parry E, Harris J, Wachsmuth R, Turner D, Bates A, Healy E, Pham-Ledard A, Beylot-Barry M, Porkert S, Mitteldorf C, Estrach T, Combalia A, Marschalko M, Csomor J, Szepesi A, Cozzio A, Dummer R, Pimpinelli N, Grandi V, Trautinger F. The PROCLIPI international registry of early-stage mycosis fungoides identifies substantial diagnostic delay in most patients. Br J Dermatol 2018; 181:350-357.
25.11.2018The PROCLIPI international registry of early-stage mycosis fungoides identifies substantial diagnostic delay in most patients
25.11.2018Br J Dermatol 2018; 181:350-357
Yoo J, Busschots A-M, Hauben E, Bervoets A, Woei-A-Jin F J S H, Matin R, Collins G, Weatherhead S, Frew J, Bayne M, Dunnill G, McKay P, Ranki A, Vakeva L, Vydianath B, Amel-Kashipaz R, Marinos L, Oikonomidi A, Stratigos A, Vignon-Pennamen M-D, Climent F, Gonzalez-Barca E, Georgiou E, Senetta R, Zinzani P, Arumainathan A, Azurdia R, Klemke C-D, Enz P, Pujol R, Quint K, Geskin L, Hong E, Evison F, Vermeer M, Cerroni L, Kempf W, Kim Y, Bur C, Folkes A, Benstead K, Twigger R, Rieger K, Brown R, Sanches J A, Miyashiro D, Akilov O, McCann S, Sahi H, Damasco F M, Querfeld C, Willemze R, Latzka J, Scarisbrick J J, Whittaker S, Nikolaou V, Tomasini C, Amitay I, Prag Naveh H, Ram-Wolff C, Battistella M, Alberti-Violetti S, Stranzenbach R, Gargallo V, Muniesa C, Child F, Guenova E, Quaglino P, Prince H M, Papadavid E, Hodak E, Bagot M, Servitje O, Berti E, Ortiz-Romero P, Stadler R, Patsatsi A, Knobler R, Koletsa T, Jonak C, Wobser M, Geissinger E, Wehkamp U, Weichenthal M, Cowan R, Parry E, Harris J, Wachsmuth R, Turner D, Bates A, Healy E, Pham-Ledard A, Beylot-Barry M, Porkert S, Mitteldorf C, Estrach T, Combalia A, Marschalko M, Csomor J, Szepesi A, Cozzio Antonio, Dummer R, Pimpinelli N, Grandi V, Trautinger F
Individualized Treatment Approaches for Langerhans Cell Histiocytosis
Roider E, Dummer R, French L, Cozzio A, Hoetzenecker W, Jochum W, Balabanov S, Kerl K, Kamarachev J, Schaller M, Metzler G, Fehrenbacher B, Signer C, Guenova E. Individualized Treatment Approaches for Langerhans Cell Histiocytosis. Br J Dermatol 2017
30.11.2017Individualized Treatment Approaches for Langerhans Cell Histiocytosis
30.11.2017Br J Dermatol 2017
Roider E, Dummer R, French L E, Cozzio Antonio, Hoetzenecker W, Jochum W, Balabanov S, Kerl K, Kamarachev J, Schaller M, Metzler G, Fehrenbacher B, Signer C, Guenova E
Comparison of pyoderma gangrenosum and hypertensive ischemic leg ulcer Martorell in a Swiss cohort
Kolios A, Hafner J, Luder C, Guenova E, Kerl K, Kempf W, Nilsson J, French L, Cozzio A. Comparison of pyoderma gangrenosum and hypertensive ischemic leg ulcer Martorell in a Swiss cohort. Br J Dermatol 2017
20.08.2017Comparison of pyoderma gangrenosum and hypertensive ischemic leg ulcer Martorell in a Swiss cohort
20.08.2017Br J Dermatol 2017
Kolios A G A, Hafner J, Luder C, Guenova E, Kerl K, Kempf W, Nilsson J, French L E, Cozzio Antonio
Unraveling a case of junctional epidermolysis bullosa in a newborn: tragic coincidence of a novel mutation of the itga6 gene and trisomic rescue
Jensen A, Cozzio A, Malzacher A, Hornung R, Hoetzenecker W, French L, Fischer T, Chang Y, Ignatova D, Rocken M, Fehrenbacher B, Schaller M, Achermann J, Traber H, Spiegel R, Bruckner-Tuderman L, Has C, Wachstein J, Guenova E (2017). Unraveling a case of junctional epidermolysis bullosa in a newborn: tragic coincidence of a novel mutation of the itga6 gene and trisomic rescue.
17.06.2017Unraveling a case of junctional epidermolysis bullosa in a newborn: tragic coincidence of a novel mutation of the itga6 gene and trisomic rescue
17.06.2017EAACI Congress 2017
Jensen AN, Cozzio A, Malzacher Andreas, Hornung René, Hoetzenecker W, French L, Fischer Tina, Chang Y, Ignatova D, Rocken M, Fehrenbacher B, Schaller M, Achermann J, Traber H, Spiegel R, Bruckner-Tuderman L, Has C, Wachstein J, Guenova E
Unexpected genetic findings in a female newborn with severe IUGR and epidermiolysis bullosa (EB)
Wachstein J, Jensen A, Spiegel R, Fischer T, Guenova E, Malzacher A (2017). Unexpected genetic findings in a female newborn with severe IUGR and epidermiolysis bullosa (EB).
01.06.2017Unexpected genetic findings in a female newborn with severe IUGR and epidermiolysis bullosa (EB)
01.06.2017Joint annual meeting SSP and SSAI 2017
Wachstein J, Jensen A, Spiegel R, Fischer Tina, Guenova E, Malzacher Andreas