Neurological aspects of osteopetrosis

Neuropathology and Applied Neurobiology

Volumn 29, Issue 2, 2003, Pages 87-97

  Steward, C G ^a  

^a Royal Hospital for Children   (United Kingdom)

Author keywords

Genes; Hypocalcaemia; Neuronal ceroid lipofuscinosis; Neuronopathic osteopetrosis; Osteoclasts; Osteopetrosis

Indexed keywords

CEROID; CHLORIDE CHANNEL; LIPOFUSCIN; PROTEIN SUBUNIT; PROTON PUMP; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE;

ACIDIFICATION; ALBERS SCHOENBERG DISEASE; ATP6I GENE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE DISORDER; BLINDNESS; BLOOD VESSEL; BONE DENSITY; BONE DISEASE; BONE GROWTH; BONE REMODELING; CAROTID ARTERY OBSTRUCTION; CLCN7 GENE; COCHLEAR NERVE; CRANIAL NERVE; DISEASE CLASSIFICATION; DISEASE SEVERITY; ENZYME DEFECT; FACIAL NERVE DISEASE; GENE; GENETIC CODE; GENETIC DISORDER; HUMAN; HYDROCEPHALUS; INTERNAL CAROTID ARTERY; METABOLIC DISORDER; NERVE DECOMPRESSION; NERVOUS SYSTEM; NEUROAXONAL DYSTROPHY; NEUROLOGIC DISEASE; OPTIC NERVE; OPTIC NERVE ATROPHY; OSTEOCLAST; PERCEPTION DEAFNESS; PRIORITY JOURNAL; PROTEIN DEFECT; PSYCHOMOTOR RETARDATION; RADIOLOGY; REVIEW; SKULL; SKULL DEVELOPMENT; SPINAL CORD; TCIRG1 GENE; TRIGEMINAL NERVE DISEASE; TUMOR SPHEROID; VEIN; VERTEBRAL ARTERY STENOSIS;

ANIMALS; BLINDNESS; CHILD; CRANIAL NERVE DISEASES; HEMATOLOGIC DISEASES; HUMANS; MODELS, ANIMAL; NERVOUS SYSTEM DISEASES; OPTIC ATROPHY; OSTEOPETROSIS; PSYCHOMOTOR DISORDERS;

EID: 0037385299     PISSN: 03051846     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2990.2003.00474.x     Document Type: Review

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