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Información de la revista
Vol. 99. Núm. 4.
Páginas 313-314 (mayo 2008)
Vol. 99. Núm. 4.
Páginas 313-314 (mayo 2008)
Letter to the Editor
Acceso a texto completo
Sturge-Weber Syndrome and Type 1 Neurofibromatosis: A Chance Association?
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7081
A.L. Rodríguez-Bujaldón, C. Vázquez-Bayo, R.J. Jiménez-Puya, J.C. Moreno-Giménez
Servicio de Dermatología Médico-Quirúrgica y Venereología, Hospital Universitario Reina Sofía, Córdoba, Spain
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References
[1.]
A. Borgberg.
Clinical and genetic investigations into tuberous sclerosis and Recklinghausen's neurofibromatosis; contribution to elucidation of interrelationship and eugenics of the syndromes.
Acta Psychiatr Neurol Scand Suppl, 71 (1951), pp. 1-239
[3.]
P. Redondo.
Malformaciones vasculares (I). Concepto, clasificación, fisiopatogenia y manifestaciones clínicas.
Actas Dermosifiliogr, 98 (2007), pp. 141-158
[4.]
S. Celebi, G. Alagöz, U. Aykan.
Ocular findings in Sturge-Weber syndrome.
Eur J Opthalmol, 10 (2000), pp. 239-243
[5.]
S. Martínez, A. Vera, A. Sanz, V. Crespo.
Neurofibromatosis segmentaria verdadera.
Actas Dermosifiliogr, 95 (2004), pp. 175-177
[6.]
R. Happle.
Klippel-Trenaunay syndrome: It is a paradominant trait?.
Br J Dermatol, 128 (1993), pp. 465-466
[7.]
W. Wertelecki, D.W. Superneau, L.W. Forehand, C.J. Hoff.
Angiomas and von Recklinghausen neurofibromatosis.
Neurofibromatosis, 1 (1988), pp. 137-145
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