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Volumn 24, Issue 4, 2007, Pages 460-462

Congenital mastocytosis associated with neurosensory deafness [14]

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHILD; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; CONGENITAL DISORDER; DISEASE ASSOCIATION; FAMILY HISTORY; FEMALE; FOLLOW UP; HUMAN; HUMAN TISSUE; LETTER; MAST CELL; MASTOCYTOSIS; NUCLEAR MAGNETIC RESONANCE IMAGING; PERCEPTION DEAFNESS; PRIORITY JOURNAL; PUNCH BIOPSY;

EID: 34548544018     PISSN: 07368046     EISSN: 15251470     Source Type: Journal    
DOI: 10.1111/j.1525-1470.2007.00489.x     Document Type: Letter
Times cited : (6)

References (10)
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  • 3
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    • Lerner, M.R.1    Lerner, A.B.2
  • 4
    • 0025090026 scopus 로고
    • Skin mastocytosis with short stature, conductive hearing loss and microtia: A new syndrome
    • Wolach B, Raas-Rothschild A, Metzker A et al. Skin mastocytosis with short stature, conductive hearing loss and microtia: a new syndrome. Clin Genet 1990 37 : 64 68.
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    • Wolach, B.1    Raas-Rothschild, A.2    Metzker, A.3
  • 5
    • 0026849463 scopus 로고
    • Skin mastocytosis, hearing loss and mental retardation
    • Hennekam RCM, Beemer FA. Skin mastocytosis, hearing loss and mental retardation. Clin Dysmorphol 1992 1 : 85 88.
    • (1992) Clin Dysmorphol , vol.1 , pp. 85-88
    • Hennekam, R.C.M.1    Beemer, F.A.2
  • 6
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    • Familial mastocytosis associated with neurosensory deafness
    • Trevisan G, Pauluzzi P, Gatti A et al. Familial mastocytosis associated with neurosensory deafness. J Eur Acad Dermatol Venerol 2000 14 : 119 122.
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    • Trevisan, G.1    Pauluzzi, P.2    Gatti, A.3
  • 7
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    • Parkinsonism due to bilateral basal ganglia lesions following mastocytosis-induced hypoxia
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    • (2004) J Neurol , vol.251 , pp. 1270-1272
    • Schramm, A.1    Grunewald, S.2    Lorenz, R.3
  • 8
    • 0034992664 scopus 로고    scopus 로고
    • Complex caryotype and absence of mutation in the c-kit receptor in aggressive mastocytosis presenting with pelvic osteolysis, eosinophilia and brain damage
    • Jost E, Michaux L, Abeele MV et al. Complex caryotype and absence of mutation in the c-kit receptor in aggressive mastocytosis presenting with pelvic osteolysis, eosinophilia and brain damage. Ann Hematol 2001 80 : 302 307.
    • (2001) Ann Hematol , vol.80 , pp. 302-307
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  • 9
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  • 10
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.