Author

Loredana Chiado'-Piat

Observed names: CHIADO'-PIAT, Loredana, Chiadò-Piat L., L Chiadò Piat, L Chiadò-Piat, L. CHIADÒ‐PIAT, L. Chiado Piat, L. Chiado-Piat, L. Chiadò Piat, L. Chiadò-Piat, L. Chiadò Piat, L. Chiadò-Piat, L. Chiad� Piat, L. Chiad�-Piat, Loredana CHIADò-Piat, Loredana Chiadò-Piat, Loredana Chiadò‐Piat, Loredana Chiadó-Piat, Loredana Chiadó‐Piat, Loredana Chiad�-Piat

Observed institutions: IRCCS Istituto Auxologico Italiano, University of Turin

OpenAlex ID: A5113496265

p145, a Protein with Associated Tyrosine Kinase Activity in a Human Gastric Carcinoma Cell Line

1988 · S Giordano, M F Di Renzo, et al. · Molecular and Cellular Biology · 83

CDKN2A/p16 inactivation in the prognosis of oligodendrogliomas

2000 · Simona Bortolotto, Loredana Chiad�-Piat, et al. · International Journal of Cancer · 60

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Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory disease

1997 · A. Migheli, T. Mongini, et al. · Neurogenetics · 57

Screening for later-onset Pompe's disease in patients with paucisymptomatic hyperCKemia

2013 · Marco Spada, Francesco Porta, et al. · Molecular Genetics and Metabolism · 56

Bcl-2 distribution in neuroepithelial tumors: an immunohistochemical study

1996 · D. Schiffer, P. Cavalla, et al. · Journal of Neuro-Oncology · 48

Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophy

1993 · Carlo Doriguzzi, Laura Palmucci, et al. · Journal of Neurology · 45

Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophy

1992 · Laura Palmucci, Carlo Doriguzzi, et al. · Journal of the Neurological Sciences · 44

Alpha-Sarcoglycan Deficiency Featuring Exercise Intolerance and Myoglobinuria

2002 · T. Mongini, C. Doriguzzi, et al. · Neuropediatrics · 33

CDKN2A/p16 in ependymomas

2001 · Simona Bortolotto, Loredana Chiadò-Piat, et al. · Journal of Neuro-Oncology · 28

Deregulation of the p14ARF/Mdm2/p53 Pathway and G1/S Transition in Two Glioblastoma Sets

2003 · Chiara Ghimenti, Valentina Fiano, et al. · Journal of Neuro-Oncology · 21

Congenital Muscular Dystrophy Associated with Familial Junctional Epidermolysis Bullosa Letalis

2008 · Carlo Doriguzzi, Laura Palmucci, et al. · European Neurology · 18

Late onset and very mild course of Xp21 Becker type muscular dystrophy.

2001 · I Bosone, S Bortolotto, et al. · PubMed · 18

Proteins phosphorylated on tyrosine as markers of human tumor cell lines

1987 · S. Giordano, M. F. Di Renzo, et al. · International Journal of Cancer · 18

Cyclin D1 expression in normal oligodendroglia and microglia cells: Its use in the differential diagnosis of oligodendrogliomas

2001 · Ivana Bosone, Paola Cavalla, et al. · Neuropathology · 17

Dystrophinopathy expressing as either cardiomyopathy or Becker dystrophy in the same family

2000 · L. Palmucci, T. Mongini, et al. · Neurology · 17

Evidence for autocrine activation of a tyrosine kinase in a human gastric carcinoma cell line

1988 · Silvia Giordano, Maria Flavia Di Renzo, et al. · Journal of Cellular Biochemistry · 17

Unusual expression and very mild course of Xp21 muscular dystrophy (Becker type) in a 60‐year‐old man with 26 percent deletion of the dystrophin gene

1994 · L. Palmucci, C. Doriguzzi, et al. · Neurology · 16

Adult onset nemaline myopathy: a distinct nosologic entity?

1993 · L Palmucci, C Doriguzzi, et al. · PubMed · 16

MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation.

2002 · T Mongini, C Doriguzzi, et al. · PubMed · 14

Clinical Spectrum of McArdle Disease: Three Cases with Unusual Expression

2008 · L. Chiadò-Piat, T. Mongini, et al. · European Neurology · 13

Differential diagnosis of vacuolar muscle biopsies: use of p62, LC3 and LAMP2 immunohistochemistry.

2017 · Elisa Vittonatto, Silvia Boschi, et al. · Europe PMC (PubMed Central) · 11

Distribution of activated caspase-3 in relation with apoptosis in human malignant gliomas

2001 · D Schiffer, V Fiano, et al. · Neuroscience Letters · 11

Systematic use of dystrophin testing in muscle biopsies: results in 201 cases

1997 · C. DORIGUZZI, L. PALMUCCI, et al. · European Journal of Clinical Investigation · 10

Myoglobinuria and carnitine palmityl transferase deficiency in father and son

1991 · T. Mongini, C. Doriguzzi, et al. · Journal of Neurology · 10

Cytochromec oxidase and coenzyme Q in neuromuscular diseases: a histochemical study

1990 · C. Doriguzzi, L. Palmucci, et al. · Acta Neuropathologica · 8

Works count: 69

Citation count: 716

H-index: 16

I10-index: 24