Ataxia-telangiectasia is a rare multisystem neurodegenerative genetic disorder due to mutation of ATM gene. The clinical expression and the immunological abnormalities are variable and apparently not associated with the type of ATM mutations. We report on two siblings affected by A-T with different clinical and immunological presentations; in particular in one the immunological phenotype was reminiscent of hyper IgM syndrome
Four cases resembling ataxia telangiectasia, all characterized by the absence of telangiectasias, ar...
SummaryWe report the spectrum of 59 ATM mutations observed in ataxia-telangiectasia (A-T) patients i...
Four cases resembling ataxia telangiectasia, all characterized by the absence of telangiectasias, ar...
Ataxia-telangiectasia is a rare multisystem neurodegenerative genetic disorder due to mutation of AT...
Ataxia-telangiectasia (A-T) is a neurodegenerative and primary immunodeficiency disorder (PID) chara...
Ataxia-telangiectasia (A-T) is characterised by progressive neurological abnormalities, oculocutaneo...
Abstract Background Ataxia telangiectasia (AT) is a rare, multi-systemic, genetic disorder. Mutation...
SummaryAtaxia-telangiectasia (A-T) is an autosomal recessive disorder characterized by cerebellar de...
Abstract Objective Variant Ataxia-Telangiectasia is caused by mutations that allow some retained AT...
Item does not contain fulltextAtaxia-telangiectasia (A-T) is an autosomal recessive neurodegenerativ...
Ataxia-telangiectasia (A-T) is an autosomal recessive neurodegenerative disorder with multisystem in...
Ataxia-telangiectasia (A-T) is an autosomal recessive neurodegenerative disorder with multisystem in...
Background Heterozygous relatives of ataxia-telangiectasia (AT) patients are at an increased risk fo...
Ataxia-telangiectasia (A-T) is a rare autosomal recessive neurodegenerative disorder. It is characte...
Ataxia telangiectasia (AT) and Nijmegen breakage syndrome (NBS) are rare autosomal recessive conditi...
Four cases resembling ataxia telangiectasia, all characterized by the absence of telangiectasias, ar...
SummaryWe report the spectrum of 59 ATM mutations observed in ataxia-telangiectasia (A-T) patients i...
Four cases resembling ataxia telangiectasia, all characterized by the absence of telangiectasias, ar...
Ataxia-telangiectasia is a rare multisystem neurodegenerative genetic disorder due to mutation of AT...
Ataxia-telangiectasia (A-T) is a neurodegenerative and primary immunodeficiency disorder (PID) chara...
Ataxia-telangiectasia (A-T) is characterised by progressive neurological abnormalities, oculocutaneo...
Abstract Background Ataxia telangiectasia (AT) is a rare, multi-systemic, genetic disorder. Mutation...
SummaryAtaxia-telangiectasia (A-T) is an autosomal recessive disorder characterized by cerebellar de...
Abstract Objective Variant Ataxia-Telangiectasia is caused by mutations that allow some retained AT...
Item does not contain fulltextAtaxia-telangiectasia (A-T) is an autosomal recessive neurodegenerativ...
Ataxia-telangiectasia (A-T) is an autosomal recessive neurodegenerative disorder with multisystem in...
Ataxia-telangiectasia (A-T) is an autosomal recessive neurodegenerative disorder with multisystem in...
Background Heterozygous relatives of ataxia-telangiectasia (AT) patients are at an increased risk fo...
Ataxia-telangiectasia (A-T) is a rare autosomal recessive neurodegenerative disorder. It is characte...
Ataxia telangiectasia (AT) and Nijmegen breakage syndrome (NBS) are rare autosomal recessive conditi...
Four cases resembling ataxia telangiectasia, all characterized by the absence of telangiectasias, ar...
SummaryWe report the spectrum of 59 ATM mutations observed in ataxia-telangiectasia (A-T) patients i...
Four cases resembling ataxia telangiectasia, all characterized by the absence of telangiectasias, ar...