Loredana Chiado'-Piat

Author

Also Known As

L Chiadò-Piat, L. CHIADÒ‐PIAT, L. Chiado-Piat, L. Chiadò-Piat, L. Chiadò-Piat, Loredana CHIADò-Piat, Loredana Chiado'-Piat, Loredana Chiadò-Piat, Loredana Chiadò‐Piat, Loredana Chiadó-Piat

Publications

573

Citations

H-Index

Concepts

All Affiliations

University of Turin Fondazione Ricerca Molinette

About

Loredana Chiado'-Piat is an author at University of Turin specializing in medicine, pathology, and mitochondrial myopathy.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	13	409
2	Health Sciences	4	4	60
3	Natural Sciences	2	2	129
4	Biochemistry	2	2	129
5	Anatomy	1	1	11

Loredana Chiado'-Piat

Publications

550

Citations

H-Index

Page 1

	Year	Citations
p145, a Protein with Associated Tyrosine Kinase Activity in a Human Gastric Carcinoma Cell Line Silvia Giordano, Maria Flavia Di Renzo, Riccardo Ferracini, Molecular and Cellular Biology Protein FunctionSignal TransductionBiochemistryCell SignalingMedicine	1988	80
Screening for later-onset Pompe's disease in patients with paucisymptomatic hyperCKemia Marco Spada, Francesco Porta, Liliana Vercelli, Molecular Genetics and Metabolism Later-onset PompeClinical EpidemiologyHematologyPathologyMedicine	2013	57
Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory disease Antonio Migheli, Tiziana Mongini, C. Doriguzzi, Neurogenetics Mitochondrial MyopathyMuscle PathologyMuscle FunctionSkeletal MuscleMedicine	1997	55
p145, a protein with associated tyrosine kinase activity in a human gastric carcinoma cell line. Silvia Giordano, Maria Flavia Di Renzo, R Ferracini, Molecular and Cellular Biology PathologyCancer BiologyTumor BiologyGastrointestinal OncologyReceptor Tyrosine Kinase	1988	49
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophy L. Palmucci, C. Doriguzzi, Tiziana Mongini, Journal of the Neurological Sciences Cardiac MuscleCardiomyopathyHeart FailurePhysiologyPathology	1992	44
Alpha-Sarcoglycan Deficiency Featuring Exercise Intolerance and Myoglobinuria Tiziana Mongini, C. Doriguzzi, Ivana Bosone, Neuropediatrics	2002	33
CDKN2A/p16 in ependymomas Simona Bortolotto, Loredana Chiado'-Piat, Paola Cavalla, Journal of Neuro-Oncology	2001	29
Deregulation of the p14ARF/Mdm2/p53 Pathway and G1/S Transition in Two Glioblastoma Sets Chiara Ghimenti, Valentina Fiano, Loredana Chiado'-Piat, Journal of Neuro-Oncology	2003	21
Congenital Muscular Dystrophy Associated with Familial Junctional Epidermolysis Bullosa Letalis C. Doriguzzi, L. Palmucci, Tiziana Mongini, European Neurology Developmental BiologySkeletal MuscleMedicineHeparan SulphateHistopathology	1993	19
Late onset and very mild course of Xp21 Becker type muscular dystrophy. Ivana Bosone, Simona Bortolotto, Tiziana Mongini, PubMed Mitochondrial MyopathyMendelian DisorderGenetic DisorderMedicinePathology	2002	18

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