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Items: 31

1.

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

Vittonatto E, Boschi S, CHIADò-Piat L, Ponzalino V, Bortolani S, Brusa C, Rainero I, Ricci F, Vercelli L, Mongini T.

Acta Myol. 2017 Dec 1;36(4):191-198. eCollection 2017 Dec.

2.

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

Spada M, Porta F, Vercelli L, Pagliardini V, Chiadò-Piat L, Boffi P, Pagliardini S, Remiche G, Ronchi D, Comi G, Mongini T.

Mol Genet Metab. 2013 Jun;109(2):171-3. doi: 10.1016/j.ymgme.2013.03.002. Epub 2013 Mar 14.

PMID:
23566438
3.

Glycogen storage disease type II diagnosed in a 74-year-old woman.

Bosone I, Vercelli L, Mongini T, Chiadó-Piat L, Vittonatto E, Palmucci L, Servidei S, Silvestri G.

J Am Geriatr Soc. 2004 Jun;52(6):1034-5. No abstract available.

PMID:
15161487
4.

Deregulation of the p14ARF/Mdm2/p53 pathway and G1/S transition in two glioblastoma sets.

Ghimenti C, Fiano V, Chiadò-Piat L, Chiò A, Cavalla P, Schiffer D.

J Neurooncol. 2003 Jan;61(2):95-102.

PMID:
12622447
5.

Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuria.

Mongini T, Doriguzzi C, Bosone I, Chiadò-Piat L, Hoffman EP, Palmucci L.

Neuropediatrics. 2002 Apr;33(2):109-11.

PMID:
12075495
6.

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

Mongini T, Doriguzzi C, Chiadò-Piat L, Silvestri G, Servidei S, Palmucci L.

Clin Neuropathol. 2002 Mar-Apr;21(2):72-6.

PMID:
12005255
7.

CDKN2A/p16 in ependymomas.

Bortolotto S, Chiadò-Piat L, Cavalla P, Bosone I, Mauro A, Schiffer D.

J Neurooncol. 2001 Aug;54(1):9-13.

PMID:
11763427
8.

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

Bosone I, Cavalla P, Chiadò-Piat L, Vito ND, Schiffer D.

Neuropathology. 2001 Sep;21(3):155-61.

PMID:
11666011
9.

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

Bosone I, Bortolotto S, Mongini T, Doriguzzi C, Chiadò-Piat L, Ugo I, Mutani R, Palmucci L.

Clin Neuropathol. 2001 Sep-Oct;20(5):196-9.

PMID:
11594504
10.

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

Schiffer D, Fiano V, Chiadò-Piat L, Mortara P, Richiardi P, Cavalla P.

Neurosci Lett. 2001 Mar 2;300(1):37-40.

PMID:
11172934
11.

CDKN2A/p16 inactivation in the prognosis of oligodendrogliomas.

Bortolotto S, Chiadò-Piat L, Cavalla P, Bosone I, Chiò A, Mauro A, Schiffer D.

Int J Cancer. 2000 Nov 15;88(4):554-7.

12.

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

Migheli A, Mongini T, Doriguzzi C, Chiadò-Piat L, Piva R, Ugo I, Palmucci L.

Neurogenetics. 1997 Sep;1(2):81-7.

PMID:
10732808
13.

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

Palmucci L, Mongini T, Chiadò-Piat L, Doriguzzi C, Fubini A.

Neurology. 2000 Jan 25;54(2):529-30. No abstract available.

PMID:
10668737
14.

Unusual clinical expression of dystrophinopathy in a female, mimicking a congenital myopathy.

Palmucci L, Doriguzzi C, Mongini T, Chiadò-Piat L, Ugo I.

Eur Neurol. 1999;42(4):221-4.

PMID:
10567819
15.

Variable histological expression of dystrophinopathy in two females.

Doriguzzi C, Palmucci L, Mongini T, Chiadò-Piat L, Saggiorato C, Ugo I, Hoffman EP.

Acta Neuropathol. 1999 Jun;97(6):657-60.

PMID:
10378386
16.

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

Doriguzzi C, Palmucci L, Mongini T, Chiadò-Piat L, Maniscalco M, Restagno G.

Eur J Clin Invest. 1997 Apr;27(4):352-8.

PMID:
9134386
17.
18.

Bcl-2 distribution in neuroepithelial tumors: an immunohistochemical study.

Schiffer D, Cavalla P, Migheli A, Giordana MT, Chiadò-Piat L.

J Neurooncol. 1996 Feb;27(2):101-9.

PMID:
8699231
19.

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.

Palmucci L, Doriguzzi C, Mongini T, Restagno G, Chiadò-Piat L, Maniscalco M.

Neurology. 1994 Mar;44(3 Pt 1):541-3.

PMID:
8145928
20.

Metachromatic dye-Ca++ATPase method in pathological muscle: a study of 382 muscle biopsies.

Doriguzzi C, Palmucci L, Mongini T, Maniscalco M, Chiadò-Piat L, De Angelis MS.

Eur J Histochem. 1994;38(1):23-8.

PMID:
7517728
21.

Adult onset nemaline myopathy: a distinct nosologic entity?

Palmucci L, Doriguzzi C, Mongini T, Chiadò-Piat L.

Clin Neuropathol. 1993 May-Jun;12(3):153-5.

PMID:
8391957
22.

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

Doriguzzi C, Palmucci L, Mongini T, Chiadò-Piat L, Restagno G, Ferrone M.

J Neurol. 1993 May;240(5):269-71.

PMID:
8326329
23.

Clinical spectrum of McArdle disease: three cases with unusual expression.

Chiadò-Piat L, Mongini T, Doriguzzi C, Maniscalco M, Palmucci L.

Eur Neurol. 1993;33(3):208-11.

PMID:
8467839
24.

Congenital muscular dystrophy associated with familial junctional epidermolysis bullosa letalis.

Doriguzzi C, Palmucci L, Mongini T, Bertolotto A, Maniscalco M, Chiadò-Piat L, Zina AM, Bundino S.

Eur Neurol. 1993;33(6):454-60.

PMID:
8307068
25.

Preferential looking techniques yield important information in strabismic amblyopia follow-up.

Brovarone FV, Fea A, Chiadò Piat L, Porro G, Ponzetto M, Cortassa F.

Doc Ophthalmol. 1993;83(4):307-12.

PMID:
8223100
26.

Preferential looking: parameters and preliminary data of a new computerized version.

Vitale Brovarone F, Fea A, Chiadò Piat L, Porro G, Ponzetto M, Amerio G.

Doc Ophthalmol. 1993;83(4):299-305.

PMID:
8223099
27.

Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophy.

Palmucci L, Doriguzzi C, Mongini T, Chiadò-Piat L, Restagno G, Carbonara A, Paolillo V.

J Neurol Sci. 1992 Sep;111(2):218-21.

PMID:
1431989
28.

Myoglobinuria and carnitine palmityl transferase deficiency in father and son.

Mongini T, Doriguzzi C, Palmucci L, Chiadò-Piat L, Maniscalco M, Schiffer D.

J Neurol. 1991 Sep;238(6):323-4.

PMID:
1940982
29.

Cytochrome c oxidase and coenzyme Q in neuromuscular diseases: a histochemical study.

Doriguzzi C, Palmucci L, Pollo B, Mongini T, Maniscalco M, Chiadò-Piat L, Schiffer D.

Acta Neuropathol. 1990;81(1):25-9.

PMID:
1964758
30.

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

Giordano S, Di Renzo MF, Narsimhan RP, Tamagnone L, Gerbaudo EV, Chiadó-Piat L, Comoglio PM.

J Cell Biochem. 1988 Dec;38(4):229-36.

PMID:
3241013
31.

p145, a protein with associated tyrosine kinase activity in a human gastric carcinoma cell line.

Giordano S, Di Renzo MF, Ferracini R, Chiadò-Piat L, Comoglio PM.

Mol Cell Biol. 1988 Aug;8(8):3510-7.

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