{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,30]],"date-time":"2026-10-30T04:13:34Z","timestamp":1793333614375,"version":"4.5.0"},"reference-count":24,"publisher":"Springer Science and Business Media LLC","issue":"11","license":[{"start":{"date-parts":[[2011,5,7]],"date-time":"2011-05-07T00:00:00Z","timestamp":1304726400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Childs Nerv Syst"],"published-print":{"date-parts":[[2011,11]]},"DOI":"10.1007\/s00381-011-1474-1","type":"journal-article","created":{"date-parts":[[2011,5,6]],"date-time":"2011-05-06T02:22:57Z","timestamp":1304648577000},"page":"1861-1865","source":"Crossref","is-referenced-by-count":7,"title":["Endoscopic third ventriculostomy for the treatment of osteopetrosis-related hydrocephalus: a case-based update"],"prefix":"10.1007","volume":"27","author":[{"given":"Bhoresh","family":"Dhamija","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Benedetta Ludovica","family":"Pettorini","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Guirish","family":"Solanki","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2011,5,7]]},"reference":[{"key":"1474_CR1","doi-asserted-by":"crossref","first-page":"103","DOI":"10.3171\/PED-08\/01\/103","volume":"1","author":"YZ Al-Tamimi","year":"2008","unstructured":"Al-Tamimi YZ, Tyagi AK, Chumas PD, Crimmins DW (2008) Patients with autosomal-recessive osteopetrosis presenting with hydrocephalus and hindbrain posterior fossa crowding. J Neurosurg Paediatrics 1:103\u2013106","journal-title":"J Neurosurg Paediatrics"},{"key":"1474_CR2","first-page":"362","volume":"98","author":"PA Baird","year":"1968","unstructured":"Baird PA, Robinson GC, Harwick DF, Sovereign AE (1968) Congenital osteopetrosis: an unusual cause of hydrocephalus. Canad Med Ass J 98:362\u2013365","journal-title":"Canad Med Ass J"},{"key":"1474_CR3","doi-asserted-by":"crossref","first-page":"263","DOI":"10.1007\/s00223-005-0027-6","volume":"77","author":"W Balemans","year":"2005","unstructured":"Balemans W, Wesenbeeck LV, Van Hul W (2005) A clinical and molecular overview of the human osteopetroses. Calcif Tissue Int 77:263\u2013274","journal-title":"Calcif Tissue Int"},{"key":"1474_CR4","first-page":"528","volume":"67","author":"H Ben Hamouda","year":"2001","unstructured":"Ben Hamouda H, Sfar MN, Braham R, Ben Saleh M, Ayadi A, Soua H, Hamza H, Sfar MT (2001) Association of severe autosomal recessive osteopetrosis and Dandy-Walker with agenesis of the corpus callosum. Acta Orthop Belg 67:528\u2013532","journal-title":"Acta Orthop Belg"},{"key":"1474_CR5","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1016\/8756-3282(88)90021-X","volume":"9","author":"J Bollerslev","year":"1988","unstructured":"Bollerslev J, Andersen PE Jr (1988) Radiological, biochemical and hereditary evidence of two types of autosomal dominant osteopetrosis. Bone 9:7\u201313","journal-title":"Bone"},{"key":"1474_CR6","doi-asserted-by":"crossref","first-page":"186","DOI":"10.1007\/s00439-002-0861-9","volume":"112","author":"AB Campos-Xavier","year":"2003","unstructured":"Campos-Xavier AB, Saraiva JM, Ribeiro LM, Munnich A, Cormier-Daire V (2003) Chloride channel 7 (CLCN7) gene mutations in intermediate autosomal recessive osteopetrosis. Hum Genet 112:186\u2013189","journal-title":"Hum Genet"},{"issue":"6","key":"1474_CR7","first-page":"1293","volume":"57","author":"J Carolino","year":"1998","unstructured":"Carolino J, Perez JA, Popa A (1998) Osteopetrosis. Am Fam Physician 57(6):1293\u20131296","journal-title":"Am Fam Physician"},{"key":"1474_CR8","doi-asserted-by":"crossref","first-page":"2861","DOI":"10.1093\/hmg\/10.25.2861","volume":"10","author":"E Cleiren","year":"2001","unstructured":"Cleiren E, B\u00e9nichou O, Van Hul E, Gram J, Bollerslev J, Singer FR, Beaverson K, Aledo A, Whyte MP, Yoneyama T, de Vernejoul MC, Van Hul W (2001) Albers-Sch\u00f6nberg disease (autosomal osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene. Hum Mol Genet 10:2861\u20132867","journal-title":"Hum Mol Genet"},{"key":"1474_CR9","first-page":"1110","volume":"21","author":"JK Cur\u00e9","year":"2000","unstructured":"Cur\u00e9 JK, Key LL, Goltra DD, Van Tassel P (2000) Cranial MR imaging of osteopetrosis. Am J Neuroradiol 21:1110\u20131115","journal-title":"Am J Neuroradiol"},{"issue":"1","key":"1474_CR10","doi-asserted-by":"crossref","first-page":"102","DOI":"10.1034\/j.1399-3046.1999.00063.x","volume":"3","author":"A Fasth","year":"1999","unstructured":"Fasth A, Porras O (1999) Human malignant osteopetrosis: pathophysiology, management and the role of bone marrow transplantation. Pediatr Transplant 3(1):102\u2013107","journal-title":"Pediatr Transplant"},{"key":"1474_CR11","doi-asserted-by":"crossref","first-page":"530","DOI":"10.3171\/ped.2004.100.5.0530","volume":"100","author":"R Grossman","year":"2004","unstructured":"Grossman R, Feldman Z (2004) Bone growth causing ventriculoperitoneal shunt malfunction in a patient with osteopetrosis. J Neurosurg (Paediatrics 5) 100:530\u2013531","journal-title":"J Neurosurg (Paediatrics 5)"},{"key":"1474_CR12","doi-asserted-by":"crossref","first-page":"205","DOI":"10.1016\/S0092-8674(01)00206-9","volume":"104","author":"U Kornak","year":"2001","unstructured":"Kornak U, Kasper D, B\u00f6sl MR, Kaiser E, Schweizer M, Schulz A, Friedrich W, Delling G, Jentsch TJ (2001) Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and men. Cell 104:205\u2013215","journal-title":"Cell"},{"issue":"9","key":"1474_CR13","first-page":"839","volume":"73","author":"DK Lam","year":"2007","unstructured":"Lam DK, Sandor GK, Holmes HI, Carmichael RP, Clokie CM (2007) Marble bone disease: a review of osteopetrosis and its oral health implications for dentists. J Can Dent Assoc 73(9):839\u2013843","journal-title":"J Can Dent Assoc"},{"key":"1474_CR14","first-page":"508","volume":"131","author":"SR Phadke","year":"2010","unstructured":"Phadke SR, Fischer B, Gupta N, Ranganath P, Kabra M, Kornak U (2010) Novel mutations in Indian patients with autosomal recessive infantile malignant osteopetrosis. Indian J Med Res 131:508\u2013514","journal-title":"Indian J Med Res"},{"issue":"7","key":"1474_CR15","doi-asserted-by":"crossref","first-page":"1194","DOI":"10.1359\/JBMR.040407","volume":"19","author":"P Quarello","year":"2004","unstructured":"Quarello P, Forni M, Barberis L, Defilippi C, Campagnoli MF, Silvestro L, Frattini A, Chalhoub N, Vacher J, Ramenghi U (2004) Severe malignant osteopetrosis caused by a GL gene mutation. J Bone Miner Res 19(7):1194\u20131199","journal-title":"J Bone Miner Res"},{"key":"1474_CR16","doi-asserted-by":"crossref","first-page":"34","DOI":"10.1097\/00003086-199309000-00005","volume":"294","author":"F Shapiro","year":"1993","unstructured":"Shapiro F (1993) Osteopetrosis. Current clinical considerations. Clin Orthop Relat Res 294:34\u201344","journal-title":"Clin Orthop Relat Res"},{"key":"1474_CR17","doi-asserted-by":"crossref","first-page":"312","DOI":"10.1038\/sj.jp.7211081","volume":"24","author":"YJ Shin","year":"2004","unstructured":"Shin YJ, Park SE, Shim GH, Lee JA, Kim EK, Park JD, Kim BI, Choi JH, Frattinin A (2004) Chloride channel CICN7 mutations in a Korean patient with infantile malignant osteopetrosis initially presenting with neonatal thrombocytopenia. J Perinatol 24:312\u2013314","journal-title":"J Perinatol"},{"key":"1474_CR18","doi-asserted-by":"crossref","first-page":"2752","DOI":"10.1073\/pnas.80.9.2752","volume":"80","author":"WS Sly","year":"1983","unstructured":"Sly WS, Hewett-Emmett D, Whyte MP, Yu YS, Tashian RE (1983) Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification. Proc Natl Acad Sci USA 80:2752\u20132756","journal-title":"Proc Natl Acad Sci USA"},{"key":"1474_CR19","doi-asserted-by":"crossref","first-page":"2371","DOI":"10.1093\/hmg\/11.20.2371","volume":"11","author":"A Smahi","year":"2002","unstructured":"Smahi A, Courtois G, Rabia SH, Doffinger R, Bodemer C, Munnich A et al (2002) The NF-kappaB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes. Hum Mol Genet 11:2371\u20132375","journal-title":"Hum Mol Genet"},{"issue":"2","key":"1474_CR20","doi-asserted-by":"crossref","first-page":"87","DOI":"10.1046\/j.1365-2990.2003.00474.x","volume":"29","author":"CG Steward","year":"2003","unstructured":"Steward CG (2003) Neurological aspects of osteopetrosis. Neuropathol Appl Neurobiol 29(2):87\u201397","journal-title":"Neuropathol Appl Neurobiol"},{"key":"1474_CR21","doi-asserted-by":"crossref","first-page":"2839","DOI":"10.1056\/NEJMra040952","volume":"351","author":"J Tolar","year":"2004","unstructured":"Tolar J, Teitelbaum SL, Orchard PJ (2004) Osteopetrosis. N Engl J Med 351:2839\u20132849","journal-title":"N Engl J Med"},{"issue":"4","key":"1474_CR22","doi-asserted-by":"crossref","first-page":"419","DOI":"10.3171\/2009.11.PEDS09370","volume":"5","author":"M Turgut","year":"2010","unstructured":"Turgut M, Aral YZ, Ozsunar Y (2010) Autosomal recessive osteopetrosis as an unusual cause of hydrocephalus, extensive calcification of tentorium cerebelli, and calvarial hyperostosis. J Neurosurg paediatr 5(4):419\u2013421","journal-title":"J Neurosurg paediatr."},{"key":"1474_CR23","first-page":"344","volume":"59","author":"WCV Venkateshwar","year":"2003","unstructured":"Venkateshwar WCV, Vaidya WCA, Roy LCP, Sampat SLS, De AVM JK (2003) Osteopetrosis. MJAFI 59:344\u2013346","journal-title":"MJAFI"},{"issue":"5","key":"1474_CR24","doi-asserted-by":"crossref","first-page":"449","DOI":"10.1136\/adc.83.5.449","volume":"83","author":"CJ Wilson","year":"2000","unstructured":"Wilson CJ, Vellodi A (2000) Autosomal recessive osteopetrosis: diagnosis, management, and outcome. Arch Dis Child 83(5):449\u2013452","journal-title":"Arch Dis Child"}],"container-title":["Child's Nervous System"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00381-011-1474-1.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s00381-011-1474-1\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00381-011-1474-1","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,6,18]],"date-time":"2020-06-18T23:09:52Z","timestamp":1592521792000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s00381-011-1474-1"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,5,7]]},"references-count":24,"journal-issue":{"issue":"11","published-print":{"date-parts":[[2011,11]]}},"alternative-id":["1474"],"URL":"https:\/\/doi.org\/10.1007\/s00381-011-1474-1","relation":{},"ISSN":["0256-7040","1433-0350"],"issn-type":[{"value":"0256-7040","type":"print"},{"value":"1433-0350","type":"electronic"}],"subject":[],"published":{"date-parts":[[2011,5,7]]}}}