Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Cristina Albarrán-Planelles"'
Autor:
Marta Rivas-Rivas, David Jiménez-Gallo, Natalia Navas-García, Cristina Albarrán-Planelles, Claudio Rodríguez-Ramos
Publikováno v:
Revista Espanola de Enfermedades Digestivas, Vol 105, Iss 10, Pp 624-625 (2013)
Externí odkaz:
https://doaj.org/article/d80af469fea3405cbe332da94a11f958
Heterozygous cylindromatosis gene mutation c.1628_1629delCT in a family with brook-spiegler syndrome
Autor:
Cintia Arjona Aguilera, Raquel De la Varga Martínez, Lidia Ossorio García, David Jimenez-Gallo, Cristina Albarrán Planelles, Mario Linares Barrios
Publikováno v:
Indian Journal of Dermatology, Vol 61, Iss 5, Pp 580-580 (2016)
Brooke–Spiegler Syndrome (BSS) is a rare genodermatosis characterized by the progressive formation of adnexal skin tumors in the scalp and face, mainly trichoepitheliomas, cylindromas, and spiradenomas. It has also been associated with salivary gla
Externí odkaz:
https://doaj.org/article/a320b395916a451cbd5f054c3f7b5af9
Autor:
María José Fernández Anguita, Mario Linares Barrios, David Jiménez Gallo, Juan Márquez Enríquez, Cristina Albarrán Planelles, María Eugenia Rodríguez Mateos
Publikováno v:
Dermatologic Therapy. 27:178-182
Pruritus is a symptom that significantly affects the patient's quality of life in cutaneous T cell lymphoma (CTCL). The most effective treatments are those that address the condition itself; however, it is often not possible to control this symptom.
Autor:
David, Jiménez-Gallo, Cristina, Albarrán-Planelles, Cintia, Arjona-Aguilera, German, Blanco-Sánchez, María Eugenia, Rodríguez-Mateos, Mario, Linares-Barrios
Publikováno v:
Dermatologic therapy. 28(3)
Thromboangiitis obliterans (TAO) or Buerger's disease is a vascular inflammatory thrombotic occlusive and segmental disease affecting distal small and medium-sized arteries of the limbs. Tobacco is the main trigger factor and avoiding it is the main
Autor:
Cristina Albarrán Planelles, Mario Linares Barrios, David Jiménez Gallo, Jose Maria Baez Baena
Publikováno v:
European Journal of Dermatology. 25:357-358
A 33-year-old man consulted for gingival hyperplasia (figure 1A) with extensive nodular lesions of progressive appearance over 20 years. They measured 5 to 10 cm, coalesced into violaceous plaques with ill-defined borders and were very indurated on p
Heterozygous cylindromatosis gene mutation c.1628_1629delCT in a family with brook-spiegler syndrome
Autor:
Mario Linares Barrios, Lidia Ossorio García, David Jiménez-Gallo, Cristina Albarrán Planelles, Cintia Arjona Aguilera, Raquel De la Varga Martínez
Publikováno v:
Indian Journal of Dermatology
Indian Journal of Dermatology, Vol 61, Iss 5, Pp 580-580 (2016)
Indian Journal of Dermatology, Vol 61, Iss 5, Pp 580-580 (2016)
Brooke–Spiegler Syndrome (BSS) is a rare genodermatosis characterized by the progressive formation of adnexal skin tumors in the scalp and face, mainly trichoepitheliomas, cylindromas, and spiradenomas. It has also been associated with salivary gla
Autor:
David, Jiménez-Gallo, Cristina, Albarrán-Planelles, Mario, Linares-Barrios, Alberto, Martínez-Rodríguez, José María, Báez-Perea, Julio Abraham, González-Fernández
Publikováno v:
Journal of cutaneous pathology. 40(9)
Lichen planus follicularis tumidus (LPFT) represents an uncommon variety of lichen planus (LP). Clinically, it presents with prominent purplish lesions or white-pigmented yellowish cysts and comedones. Histopathologically, it is similar to lichen pla