Pages that link to "Q42514825"

The following pages link to Cerebellar ataxia associated with heteroallelic ceruloplasmin gene mutation (Q42514825):

Displaying 23 items.

• Diagnosis and management of early- and late-onset cerebellar ataxia (Q31089826) (← links)
• Iron metabolism in Parkinsonian syndromes (Q33248678) (← links)
• Neurodegeneration with brain iron accumulation — Clinical syndromes and neuroimaging (Q33969371) (← links)
• Identification of mineral deposits in the brain on radiological images: a systematic review (Q34300363) (← links)
• Iron in neurodegenerative disorders (Q35112542) (← links)
• Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation. (Q35596505) (← links)
• Aceruloplasminemia: an inherited neurodegenerative disease with impairment of iron homeostasis (Q35754529) (← links)
• A diagnostic approach for neurodegeneration with brain iron accumulation: clinical features, genetics and brain imaging. (Q36093991) (← links)
• Protective role of macrophage-derived ceruloplasmin in inflammatory bowel disease. (Q36677029) (← links)
• Copper handling machinery of the brain (Q37808945) (← links)
• Single-nucleotide polymorphisms and haplotypes of non-coding area in the CP gene are correlated with Parkinson's disease (Q38901449) (← links)
• Genetics and Pathophysiology of Neurodegeneration with Brain Iron Accumulation (NBIA). (Q41836301) (← links)
• Astrocytic deformity and globular structures are characteristic of the brains of patients with aceruloplasminemia (Q42528707) (← links)
• Vermal atrophy of alcoholics correlate with serum thiamine levels but not with dentate iron concentrations as estimated by MRI. (Q46391734) (← links)
• Perinatal copper deficiency alters rat cerebellar purkinje cell size and distribution (Q47172067) (← links)
• Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia. (Q47355024) (← links)
• Synchrotron X-ray fluorescence reveals abnormal metal distributions in brain and spinal cord in spinocerebellar ataxia: a case report (Q48691950) (← links)
• Loss of NCB5OR in the cerebellum disturbs iron pathways, potentiates behavioral abnormalities, and exacerbates harmaline-induced tremor in mice (Q48730588) (← links)
• Extrapyramidal and cerebellar movement disorder in association with heterozygous ceruloplasmin gene mutation (Q49140950) (← links)
• Biochemical features of ceruloplasmin gene mutations linked to aceruloplasminemia (Q51806779) (← links)
• Aceruloplasminemia: Waiting for an Efficient Therapy (Q60046955) (← links)
• Multiple motor system dysfunction associated with a heterozygous ceruloplasmin gene mutation (Q80753921) (← links)
• Predominant ataxia, low ceruloplasmin, and absent K–F rings: Hypoceruloplasminemia or Wilson's disease (Q84984275) (← links)