Results 151 to 160 of about 36,363 (277)

Enamel Defects in Carriers of a Novel LAMA3 Mutation Underlying Epidermolysis Bullosa [PDF]

, 2012
Jonkman, MF, Pasmooij, AM, Stellingsma, C, Yuen, WY   +3 more
core   +2 more sources

Epidermolysis Bullosa [PDF]

Proceedings of the Royal Society of Medicine, 1933
openaire   +2 more sources

Atención enfermera al paciente pediátrico con epidermolisis bullosa. Revisión bibliográfica [PDF]

, 2019
INTRODUCCIÓN. La epdiermólisis bullosa (EB) es una enfermedad de baja prevalencia, perteneciente a las genodermatosis de etiología genética, que se caracteriza por la deficiencia parcial o total de alguna de las proteínas que conforman los estratos ...
Blanco Asensio, Elena
core  

Metaplastic Conditions in The Bladder in Patient With Epidermolysis Bullosa

International Brazilian Journal of Urology
Epidermolysis bullosa is a rare inherited muco-cutaneous disorder that sometimes presents with genitourinary involvement. Herein we report the case of an 11-year-old girl with a history of junctional epidermolysis bullosa who was admitted with urological
Kenan Yilmaz, Deniz Demirci, Numan Baydilli, Sinan Nazlim   +3 more
doaj   +1 more source

Epidermolysis Bullosa [PDF]

Proceedings of the Royal Society of Medicine, 1945
openaire   +2 more sources

Suramin for treatment of adrenocortical carcinoma [PDF]

, 1989
Allolio, B, Arlt, W, Deuss, U, Reincke, M, Siekmann, L, Winkelmann, W   +5 more
core   +1 more source

Epidermolysis Bullosa: Two rare case reports of COL7A1 and EBS-GEN SEV KRT14 variants with review of literature

BMC Pediatrics
Epidermolysis Bullosa is a rare hereditary skin condition that causes blisters. Genes encoding structural proteins at or near the dermal-epidermal junction are mutated recessively or dominantly, and this is the primary cause of EB.
Fatma Mabrouk Ali, Jieyu Zhou, Mingyan Wang, Qiuxia Wang, Lulu Sun, Mansour Maulid Mshenga, Hongyan Lu   +6 more
doaj   +1 more source

Epidermolysis Bullosa [PDF]

Archives of Disease in Childhood, 1954
openaire   +2 more sources

The potential of human induced pluripotent stem cells for modelling diabetic wound healing in vitro [PDF]

, 2018
Aasen, Abaci, Abaci, Agha, Ahmed, Ahmed, Al-Awar, American Diabetes Association, Amoh, Annette Graham, Ansell, Ansell, Baltzis, Bielefeld, Bilousova, Blaber, Brouwer, Burkart, Burnett, Buta, Buth, Buth, Catherine S. Wright, Ceder, Chan, Chen, Chichagova, Cory, Davidson, Drawnel, Erin M. O’Shaughnessy, Faller, Faniku, Frank, Fujikura, Gerami-Naini, Girard, Gledhill, Golebiewska, Griscelli, Griscelli, Groeber, Guo, Gurdon, Gurdon, Gurdon, Harvey, Hattersley, Hewitt, Hirsch, Hosokawa, Hu, Hu, Hu, Ianitti, Itoh, Itoh, Kandyba, Kim, Kim, Kogut, Kong, Kwak, Laakso, Lapasset, Levitsky, Li, Liu, Loo, Lotte, Maherali, Maione, Mansbridge, Marion, Marro, Martin, Martinez-Santamaria, Martinez-Santamaria, Matsubara, McCormick, Mewes, Mirza, Mori, Morran, Nissan, Nissan, Nunan, Pane, Park, Patni, Patricia E. Martin, Paull, Peloso, Pennarossa, Peppa, Petrova, Pollok, Prigione, Prodinger, Pugliese, Rajaei, Rittie, Roquet, Rostovskaya, Ruiz, Saarimaki-Vire, Sacks, Salvotelli, Schonberger, Schuster, Seah, Shanmugam, Sharpe, Shi, Shtrichman, Siller, Siller, Siller, Singh, Stagi, Steinberg, Steinle, Sugimoto, Sun, Takahashi, Takahashi, Takahashi, Teo, Teo, Toustrup, Tsourdi, Utikal, Van den Broek, Veraitch, Von Joest, Wallet, Wang, Wenzel, Wicks, Wiegland, Wright, Wright, Wright, Yabe, Yang, Yazdanpanah, Young, Yu, Zaccardi, Zhang, Zomer   +150 more
core   +1 more source

Esophagitis and almost complete esophageal occlusion in a girl with epidermolysis bullosa

The Turkish Journal of Pediatrics, 2012
Epidermolysis bullosa is a genetically transmitted skin disorder that typically manifests with trauma-induced skin blistering, scarring and in some cases mucosal involvement. Esophageal webs, strictures or stenosis can be found in about a third of
Zlatko Djurić, Aleksandar Nagorni, Dragoljub Zivanović   +2 more
doaj