- Fanconi Anemia and Ataxia Telangiectasia in Siblings who Inherited Unique Combinations of Novel FANCA and ATM Null Mutations.
- Genetic analysis of undiagnosed ataxia-telangiectasia-like disorders.
- Genotype, extrapyramidal features and severity of variant Ataxia-Telangiectasia.
- Growth and nutrition in children with ataxia telangiectasia.
- Ibuprofen prevents progression of ataxia telangiectasia symptoms in ATM-deficient mice.
- In vivo effects of dexamethasone on blood gene expression in ataxia telangiectasia.
- Inactive Atm abrogates DSB repair in mouse cerebellum more than does Atm loss, without causing a neurological phenotype.
- Inflammation, a significant player of Ataxia-Telangiectasia pathogenesis?
- K63-linked polyubiquitin chains bind to DNA to facilitate DNA damage repair.
- Long-term nutritional and gastrointestinal aspects in patients with ataxia telangiectasia.
- Malignant Peritoneal Mesothelioma in an Infant With Familial ATM Mutations.
- Medical Management of Pediatric Malignant Bowel Obstruction in a Patient with Burkitt's Lymphoma and Ataxia Telangiectasia Using Continuous Ambulatory Drug Delivery System.
- Minimum effective betamethasone dosage on the neurological phenotype in patients with ataxia-telangiectasia: a multicenter observer-blind study.
- Mitochondrial redox sensing by the kinase ATM maintains cellular antioxidant capacity.
- Modulation of chromatin conformation by the histone deacetylase inhibitor trichostatin A promotes the removal of radiation-induced lesions in ataxia telangiectasia cell lines.
- Modulation of hypersensitivity to oxidative DNA damage in ATM defective cells induced by potassium bromate by inhibition of the Poly (ADP-ribose) polymerase (PARP).
- More than ataxia - Movement disorders in ataxia-telangiectasia.
- Neurodegeneration in ataxia-telangiectasia: Multiple roles of ATM kinase in cellular homeostasis.
- Neurovisual Assessment in Children with Ataxia Telangiectasia.
- P 111 - Rehabilitation results in children with ataxia telengiectasia: three case reports.
