Results 31 to 40 of about 81,034 (193)

Clinical periodontal diagnosis

Periodontology 2000, EarlyView., 2023
Abstract Periodontal diseases include pathological conditions elicited by the presence of bacterial biofilms leading to a host response. In the diagnostic process, clinical signs such as bleeding on probing, development of periodontal pockets and gingival recessions, furcation involvement and presence of radiographic bone loss should be assessed prior ...
Giovanni E. Salvi, Andrea Roccuzzo, Jean‐Claude Imber, Alexandra Stähli, Björn Klinge, Niklaus P. Lang   +5 more
wiley   +1 more source

Epidermolysis Bullosa Simplex

Journal of the Dermatology Nurses' Association, 2022
ABSTRACT Epidermolysis bullosa simplex (EBS) is a rare autosomal dominant, genetic condition where bullous lesions, larger than 0.5 cm, affect an area of the skin that is exposed to mechanical friction or minor trauma. Prevention of the bullous lesions starts with family and patient education, with infants requiring greater care and control ...
Tammy Sadighi, Cheryl Swayne
openaire   +2 more sources

Correlation between nutritional, hematological and infectious characteristics and classification of the type of epidermolysis bullosa of patients assisted at the Dermatology Clinic of the Hospital Universitário de Brasília [PDF]

Anais Brasileiros de Dermatologia, 2015
: Epidermolysis bullosa comprises a group of phenotypically different genodermatosis, hereditary or acquired, characterized by skin fragility and subsequent formation of blisters in response to mechanical trauma, and which may also affect mucous ...
Márcia Carolline dos Santos Sousa, Carmen Dea Ribeiro de Paula, Pedro Luiz Tauil, Izelda Maria Carvalho Costa   +3 more
doaj   +1 more source

Mutation detection and correction experiments in epidermolysis bullosa simplex [PDF]

, 2002
This thesis deals with DNA diagnosis of epidermolysis bullosa simplex (EBS) and a potential gene therapeutic approach of this ...
Schuilenga-Hut, Petra Henriette Lidia
core   +19 more sources

Generation of a human induced pluripotent stem cell line (UQACi001-A) from a severe epidermolysis bullosa simplex patient with the heterozygous mutation p.R125S in the KRT14 gene

Stem Cell Research, 2020
We have generated UQACi001-A, a new induced pluripotent stem cell (iPSC) line derived from skin fibroblasts of a male patient with the generalized severe epidermolysis bullosa simplex phenotype (EBS-gen sev) and carrying the keratin 14 (K14) R125S ...
Mbarka Bchetnia, Laurie Martineau, Véronique Racine, Julie Powell, Catherine McCuaig, Jack Puymirat, Catherine Laprise   +6 more
doaj   +1 more source

Epidermolysis Bullosa in Calves in the United Kingdom [PDF]

, 2010
Epidermolysis bullosa (EB) was diagnosed in eight calves from four farms in the United Kingdom on the basis of clinical, histological and ultrastructural findings. In three affected herds, pedigree Simmental bulls had been mated with Simmental-cross cows.
Skuse, A.M., Philbey, A W, Higgins, R J, Fraser, M., Thompson, H., Higgins, R.J., Day, M J, Foster, A.P., Higgins, R. J., Fraser, M.A., Day, M.J., Philbey, A. W., Thomson, J., Skuse, A M, Fraser, M A, Philbey, A., Foster, A P, Bowden, P E, Bowden, P.E., Barrett, D. C., Thomson, J. R., Bowden, P. E., Fraser, Mary, Day, M. J., Thomson, J R, Thompson, H, Barrett, D C, Fraser, M. A., Barrett, D.C., Skuse, A. M., Bowden, Paul Edward, Foster, A. P.   +31 more
core   +1 more source

Epidermólisis bullosa en España: Estudio observacional de una cohorte de pacientes atendidos en un centro de referencia nacional

Actas Dermo-Sifiliográficas, 2021
Resumen: Antecedentes y objetivo: La epidermólisis bullosa (EB) es un grupo heterogéneo de trastornos hereditarios caracterizado por un aumento de la fragilidad mucocutánea.
R. Maseda Pedrero, L. Quintana Castanedo, I. Pérez Conde, M. Jiménez González, M.J. Escámez Toledano, R. de Lucas Laguna   +5 more
doaj   +1 more source

Inheritance of the Epidermolysis Bullosa Subtypes [PDF]

, 2023
Epidermolysis bullosa (EB) is a group of inherited disorders that cause skin to blister and tear easily. The disease is caused by mutations in structural proteins that are key for maintaining the integrity of the skin’s basement membrane zone or ...
Beadini, Nexbedin, Elezi, Nevzat, Zhaku, Vegim, Bilalli, Sefedin, Uzeiri-Havziu, Crita, Beadini, Albulena, Alija, Gjylai, Temaj, Anjeza, Nuhii, Nexhibe, Elezi, Ron, Beadini, Sheqibe, Haxhiu- Zajmi, Arlinda, Gashi, Yllka, Shabani, Arjeta   +13 more
core   +1 more source

Genetic Profile of Epidermolysis Bullosa Cases in King Abdulaziz Medical City, Riyadh, Saudi Arabia

Frontiers in Genetics, 2022
Epidermolysis bullosa (EB) is a rare heterogeneous genetic mechanobullous skin disorder that is characterized by increased skin fragility leading to blistering following minor trauma. EB may be inherited as an autosomal dominant or an autosomal recessive
Raghad Alharthi, Raghad Alharthi, Muhannad A. Alnahdi, Muhannad A. Alnahdi, Ahad Alharthi, Seba Almutairi, Seba Almutairi, Sultan Al-Khenaizan, Sultan Al-Khenaizan, Mohammed A. AlBalwi, Mohammed A. AlBalwi, Mohammed A. AlBalwi   +11 more
doaj   +1 more source

Epidermolysis bullosa simplex: A case report [PDF]

, 2012
Epidermolysis bullosa (EB) is a rare hereditary cutaneous disorder inherited mainly in an autosomal dominant fashion. It consists of a group of conditions that cause the skin to be fragile and blister easily.
Omene, J, Akinbami, FO, Kunle-Olowu, OE, Peterside, O, Adeyemi, OO   +4 more
core   +1 more source