I-cell disease (mucolipidosis Ii or sialidosis
Baggio, P.
Minerva Pediatrica 30(11): 865-884
1978
ISSN/ISBN: 0026-4946 PMID: 353485 Document Number: 125176
Document emailed within 1 workday
Related Documents
Durand, P.; Gatti, R.; Cavalieri, S.; Borrone, C.; Tondeur, M.; Michalski, J.C.; Strecker, G. 1977: Sialidosis (mucolipidosis I) Helvetica Paediatrica Acta 32(4-5): 391-400Farriaux, J.P.; Walbaum, R.; Hongre, J.F.; Dubois, O.; Louis, J.; Blanckaert, D.; Dhondt, J.L.; Richard, P.; Fontaine, G. 1976: Mucolipidosis Ii or i cell disease. Critical review and study of 5 personal observations Lille Medical: Journal de la Faculte de Medecine et de Pharmacie de l'Universite de Lille 21(1): 51-70
Kozlowski, K.; Lipson, A.; Carey, W. 1991: Mild I-cell disease, or severe pseudo-Hurler polydystrophy in three siblings: further evidence for intermediate forms of mucolipidosis Ii and III. Radiological features La Radiologia Medica 82(6): 847-851
Ovali, F.; Samanci, N.; Güray, A.; Akdoğan, Z.; Akdeniz, C.; Dağoğlu, T.; Petorak, I. 1998: Congenital sialidosis Turkish Journal of Pediatrics 40(3): 447-451
Matsuzaki, K.; Matsumoto, Y.; Yoshihara, W.; Okada, S.; Midorikawa, M.; Inui, K.; Yutaka, T.; Yamano, T. 1987: A case of infantile sialidosis associated with congenital chylous ascites No to Hattatsu 19(3): 249-253
Kuriyama, M.; Ariga, T.; Ando, S.; Suzuki, M.; Yamada, T.; Miyatake, T. 1981: Urinary sialyloligosaccharides in adult type sialidosis: occurrence of two positional isomers Japanese Journal of Experimental Medicine 51(2): 129-132
Fukunaga, H.; Hirose, K.; Beppu, H.; Uono, M.; Suzuki, Y. 1976: 2 siblings with mucolipidosis Rinsho Shinkeigaku 16(8): 566-573
Somford, M.P.; Vanhoenacker, F.M.; Draijer, W.E.; Kort, N.P.; Thomassen, B.J. 2009: Skeletal deformities in mucolipidosis IIi Jbr-Btr: Organe de la Societe Royale Belge de Radiologie 92(3): 168-169
Ligutić, I.; Barisić, I.; Fumić, K.; Sabados, M. 1996: Mucolipidosis type III (case report) Lijecnicki Vjesnik 118(1-2): 17-20
Morava, E.; Eduard, P.; Tóth, G.áb.; Dobos, M.; Melegh, B.él.; Kosztolányi, G.ör. 2002: Mucolipidosis Ii with unusual biochemical parameters Orvosi Hetilap 143(3): 135-137
Choulot, J.J.; Théophile, D.; Saint-Martin, J.; Netter, J.C.; Petrus, M. 1988: Fetal ascites as a manifestation of atypical mucolipidosis Annales de Pediatrie 35(10): 757-758
Owada, M. 1984: Hereditary connective tissue diseases. Mucolipidosis Nihon Rinsho. Japanese Journal of Clinical Medicine 42(5): 1095-1103
Hieber, V.; Distler, J.; Jourdian, G.W.; Schmickel, R. 1975: Accumulation of 32S-mucopolysaccharides in cultured mucolipidosis cells Birth Defects Original Article Series 11(6): 307-310
Orii, T.; Nakao, T. 1974: A new type of mucolipidosis with beta-galactosidase dificiency and glycopeptiduria Jinrui Idengaku Zasshi. Japanese Journal of Human Genetics 19(1): 61-62
Colome, M.F.; Olewniczak, G.; Gallet, M.; Tiberghien, J.P.; Krim, G.; Piussan, C.; Risbourg, B. 1985: Radiological case of the month. Type II mucolipidosis with neonatal disclosure Archives Francaises de Pediatrie 42(7): 539-540
Ejiri, M.; Watanabe, T.; Ueta, Y.; Koseki, M. 1983: Detection of mucopolysaccharidosis and mucolipidosis by quantitative and qualitative analyses of urinary complex carbohydrates Rinsho Byori. Japanese Journal of Clinical Pathology 31(3): 336-340
Simsek-Kiper, P.O.; Topaloglu, R.; Sahin, Y.; Utine, G.E.; Boduroglu, K. 2013: Mucolipidosis type IIi in an adolescent presenting with atypical facial features and skeletal deformities Genetic Counseling 24(1): 7-12
Hall, V.J. 2008: Embryonic stem cells and Parkinson's disease: cell transplantation to cell therapy Annals of the Academy of Medicine Singapore 37(3): 163
Lamperi, S.; Carozzi, S. 1984: CAPD and bone marrow cell-cell interaction abnormality in end stage renal disease International Journal of Artificial Organs 7(2): 57-62
Acabá, L.; Santiago, N.; Vélez García, E. 1996: T-cell rich B-cell lymphoma masquerading as Hodgkin disease: excellent outcome to inadequate therapy Boletin de la Asociacion Medica de Puerto Rico 88(4-6): 32-34