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Volumn 36, Issue 1, 2005, Pages 21-34

Earliest clinical manifestations and natural history of neurofibromatosis type 2 (NF2) in childhood: A study of 24 patients

Author keywords

Early onset; Neurofibromatosis; NF2; Paediatric

Indexed keywords

ACOUSTIC NEURINOMA; ADOLESCENT; ADULT; AMBLYOPIA; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAIN STEM TUMOR; CAFE AU LAIT SPOT; CATARACT; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CRANIAL NERVE; CRANIAL NEUROPATHY; DISEASE ACTIVITY; DISEASE COURSE; EAR INFECTION; EYE DISEASE; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HEARING LOSS; HOARSENESS; HUMAN; HUMAN TISSUE; ITALY; MALE; MENINGIOMA; MOLECULAR GENETICS; NERVOUS SYSTEM TUMOR; NEUROFIBROMATOSIS; NEUROLOGIC DISEASE; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL; PROSPECTIVE STUDY; RETROSPECTIVE STUDY; SEIZURE; SKIN TUMOR; STRABISMUS; TINNITUS; BRAIN; COMPARATIVE STUDY; EAR NOSE THROAT DISEASE; EYE MOVEMENT DISORDER; FAMILY HEALTH; FOLLOW UP; GENETICS; METHODOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; PATHOLOGY; PATHOPHYSIOLOGY; PRESCHOOL CHILD; SPINAL CORD;

EID: 21044447532     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-837581     Document Type: Article
Times cited : (114)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.