Annalinda Pisano | Ricerc@Sapienza

Pubblicazioni

Titolo	Pubblicato in	Anno
Neuromuscular magnetic stimulation counteracts muscle decline in ALS patients: results of a randomized, double-blind, controlled study	SCIENTIFIC REPORTS	2019
Breast cancer subtypes affect the nodal response after neoadjuvant chemotherapy in locally advanced breast cancer: Are we ready to endorse axillary conservation?	THE BREAST JOURNAL	2019
Novel compound mutations in the mitochondrial translation elongation factor (TSFM) gene cause severe cardiomyopathy with myocardial fibro-adipose replacement	SCIENTIFIC REPORTS	2019
CD73 expression and pathologic response to neoadjuvant chemotherapy in triple negative breast cancer	VIRCHOWS ARCHIV	2019
Anti-aminoacyl-tRNA synthetase-related myositis and dermatomyositis: clues for differential diagnosis on muscle biopsy	VIRCHOWS ARCHIV	2018
Cerebral mitochondrial microangiopathy leads to leukoencephalopathy in mitochondrial neurogastrointestinal encephalopathy	AJNR, AMERICAN JOURNAL OF NEURORADIOLOGY	2018
Can IDO activity predict primary resistance to anti-PD-1 treatment in NSCLC?	JOURNAL OF TRANSLATIONAL MEDICINE	2018
Potential role for the VDR agonist elocalcitol in metabolic control: evidences in human skeletal muscle cells	JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY	2017
Impaired mitochondrial biogenesis is a common feature to myocardial hypertrophy and end-stage ischemic heart failure	CARDIOVASCULAR PATHOLOGY	2016
Short peptides from leucyl-tRNA synthetase rescue disease-causing mitochondrial tRNA point mutations	HUMAN MOLECULAR GENETICS	2016
Nonischemic left ventricular scar and cardiac sudden death in the young	HUMAN PATHOLOGY	2016
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy	EMBO MOLECULAR MEDICINE	2015
Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy	HUMAN MOLECULAR GENETICS	2015