Clinical study of 2 cases of Sturge-Weber-Krabbe syndrome
Kazemi, D.J.; Famili, H.
Acta Medica Iranica 19(3): 231-234
1976
ISSN/ISBN: 0044-6025 PMID: 1032452 Document Number: 106840
Document emailed within 1 workday
Related Documents
Feng, Y.K.; Yang, Y.C. 1980: Sturge-Weber syndrome: a report of 22 cases Chinese Medical Journal 93(10): 697-708Yukimori, E. 1971: Hemangiomatosis of the choroid in Sturge-Weber's syndrome. a fluorographic study Nippon Ganka Gakkai Zasshi 75: 619-626
Sinawat, S.; Auvichayapat, N.; Auvichayapat, P.; Yospaiboon, Y.; Sinawat, S. 2014: 12-year retrospective study of Sturge-Weber syndrome and literature review Journal of the Medical Association of Thailand 97(7): 742-750
Ortonne, J.P.; Floret, D.; Coiffet, J.; Cottin, X. 1978: Ocular and cutaneous melanosis associated with the Sturge-Weber syndrome: clinical, histological, and ultrastructural studies of one case Annales de Dermatologie et de Venereologie 105(12): 1019-1031
Chaturvedi, P.; Sahare, P.; Banait, N. 1999: Sturge Weber syndrome Indian Pediatrics 36(1): 91
Umar, S.H.; Glenn, M. 2000: Case presentation: Sturge-Weber Syndrome Journal of the National Medical Association 92(5): 261-262
Nagy, G.; Dósa, M. 1985: Inverse type Sturge-Weber syndrome Dermatologische Monatschrift 171(6): 395-400
Happle, R. 2003: Sturge-Weber-Klippel-Trenaunay syndrome: what's in a name? European Journal of Dermatology: Ejd 13(3): 223
Manzitti, E.; Cocucci, D.; De Mayorga, E.C.; Carrion, R. 1972: Klippel-Trenaunay syndrome and its relation to the Sturge-Weber encephalo-trigeminal angiomatosis syndrome Prensa Medica Argentina 59(9): 340-343
Stokes, A.C.; Hernández-Cossio, O.; Hernández-Fustes, O.J.; Munhoz, R.P.; Hernández-Fustes, O.J.; Francisco, A.N. 2000: Sturge-Weber syndrome: differential diagnosis of neurocysticercosis Revista de Neurologia 30(1): 41-44
Sarwar, M. 1977: Deep venous occlusion in the Sturge-Weber syndrome Revista Interamericana de Radiologia 2(3): 159-161
Tomás-Vila, M.; Menor-Serrano, F.; Arcos-Machancoses, J.é V.; García-Camuñas, Y.; Pitarch-Castellanos, I.; Barbero, P. 2013: Transient focal deficits in children with Sturge-Weber syndrome Revista de Neurologia 56(4): 253-255
Furukawa, T.; Igata, A.; Toyokura, Y. 1970: Ikeda S: Sturge-Weber and Klippel-Trénaunay syndrome with nevus of ota and ito Archives of Dermatology 102(6): 640-645
Chaithirayanon, S.; Boonyaleephan, S.; Treesirichod, A.; Siripornpanich, V. 2013: Early onset and rapid progression of glaucoma in a neonate with Sturge-Weber syndrome Journal of the Medical Association of Thailand 96(3): 374-377
Wong, H.Seng.; Abdul Rahman, R.; Choo, S.Ying.; Yahya, N. 2012: Sturge-Weber-Syndrome with extreme ocular manifestation and rare association of upper airway angioma with anticipated difficult airway Medical Journal of Malaysia 67(4): 435-437
Kopyść, Z.; Izmajlowicz, I. 1970: Mixed form of neuroectomesodermal dysplasia with features of Sturge-Weber and Klippel-Trenaunay syndromes Wiadomosci Lekarskie 23(7): 575-579
Dulac, O.; Larregue, M.; Roger, J.; Arthuis, M. 1982: Sturge-Weber disease: value of the topographic analysis of the facial angioma for the diagnosis of associated pial angioma Archives Francaises de Pediatrie 39(3): 155-158
Lupo, I.; Aiello, F.; Aiello, G.; La Rocca, M.; Reina, C.; Piccoli, F. 1987: A case of "Milles variant" of the Sturge-Weber disease with von Hippel-Lindau defective disease Acta Neurologica 9(5-6): 328-333
Schwab, W.; Hofstädter, F. 1983: Pfeifer-Weber-Christian syndrome of the mesentery. Clinical and pathologico-anatomical aspects Acta Medica Austriaca 10(1): 25-29
Figols, J.; Zimmer, C.; Warzok, R.; Cervos-Navarro, J. 1992: Immuno-lectin histochemistry and ultrastructure in two cases of globoid cell leukodystrophy (Krabbe's disease) Clinical Neuropathology 11(6): 312-317