CINECA IRIS Institutional Research Information System

PALMUCCI, Laura Maria
 Distribuzione geografica
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Continente #
NA - Nord America 2.039
EU - Europa 1.994
AS - Asia 722
AF - Africa 17
Continente sconosciuto - Info sul continente non disponibili 5
SA - Sud America 3
OC - Oceania 2
Totale 4.782
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Nazione #
US - Stati Uniti d'America 1.972
CN - Cina 426
UA - Ucraina 329
SE - Svezia 302
IE - Irlanda 253
DE - Germania 249
FR - Francia 162
IT - Italia 162
FI - Finlandia 149
AT - Austria 145
KR - Corea 145
GB - Regno Unito 136
SG - Singapore 86
CA - Canada 66
PL - Polonia 45
VN - Vietnam 26
IN - India 19
BE - Belgio 13
SN - Senegal 12
RS - Serbia 11
ES - Italia 7
GR - Grecia 7
RU - Federazione Russa 6
UZ - Uzbekistan 6
EU - Europa 5
JP - Giappone 4
NL - Olanda 4
NO - Norvegia 4
RO - Romania 4
PK - Pakistan 3
TN - Tunisia 3
AU - Australia 2
BR - Brasile 2
CZ - Repubblica Ceca 2
IR - Iran 2
MU - Mauritius 2
MY - Malesia 2
TH - Thailandia 2
CH - Svizzera 1
EE - Estonia 1
IL - Israele 1
MX - Messico 1
PT - Portogallo 1
SI - Slovenia 1
UY - Uruguay 1
Totale 4.782
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Città #
Chandler 384
Beijing 376
Dublin 253
Jacksonville 177
Vienna 144
Nyköping 113
Ann Arbor 103
Villeurbanne 82
Princeton 75
Dearborn 66
Ashburn 65
Houston 64
Medford 64
Milan 58
Boston 50
Singapore 47
Warsaw 45
Verona 44
Fairfield 36
Boardman 32
Wilmington 32
Lachine 29
Toronto 24
Dong Ket 18
Woodbridge 18
Cambridge 13
Detroit 12
Norwalk 12
Fremont 11
Ottawa 11
Brussels 9
Redmond 9
Falls Church 8
Guangzhou 8
Santa Clara 8
Hefei 7
Mountain View 7
Munich 7
Nanjing 7
Redwood City 7
Chicago 6
Düsseldorf 5
Egham 5
Kunming 5
Madrid 5
New York 5
Torino 5
Washington 5
Athens 4
Auburn Hills 4
Belgrade 4
Los Angeles 4
Pune 4
Seattle 4
Turin 4
Bologna 3
Changsha 3
Cincinnati 3
Como 3
Craiova 3
Hebei 3
Modena 3
Naples 3
Rahim 3
Silver Spring 3
Tokyo 3
Zaventem 3
Bangkok 2
Baotou 2
Bitonto 2
Bollengo 2
Caserta 2
Denver 2
Dronten 2
Edinburgh 2
Etnedal 2
Ferrara 2
Fuzhou 2
Hangzhou 2
Helsinki 2
Nanchang 2
Ningbo 2
Paris 2
Philadelphia 2
Pompei 2
Rivoli 2
Rome 2
Ruma 2
Shanghai 2
Springfield 2
Stavanger 2
Tappahannock 2
University Park 2
Alicante 1
Ardabil 1
Berkeley 1
Bitetto 1
Borgomanero 1
Bottmingen 1
Carcavelos 1
Totale 2.699
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Nome #
Chinese red rice depletes muscle coenzyme Q10 and maintains muscle damage after discontinuation of statin treatment 153
X-linked Charcot-Marie-Tooth polyneuropathy due to mutation of the connexin-32 gene: revision of our cases of genetic neuropathies and identification of three affected families. 123
Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuria. 118
A defective L_MAG (large myelin-associated glycoprotein) is responsible for an adult-onset autosomal dominant orthochromatic leukodystrophy 105
Muscular involvement in Whipple's disease with gastrointestinal sparing 104
Central core disease: histochemical and ultrastructural study of muscle biopsies of father and daughter. 97
Analysis of some factors effecting survival in malignant gliomas. 93
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency 92
Spongiform encephalopathy in addicts inhaling pre-heated heroin. 87
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. 87
Adult onset nemaline myopathy: a distinct nosologic entity? 84
La distrofia muscolare oculo-faringea: caratteristiche cliniche e genetiche 84
Sporadic ulcerative mutilating acropathy with imbalance of free amino acids in the cerebrospinal fluid. 83
Absence of dystrophin in two patients with Becker type Xp21 muscular dystrophy. 83
Systematic use of dystrophin testing in muscle biopsies: results in 201 cases. 83
Clinical spectrum of McArdle disease: three cases with unusual expression. 83
Myelin-associated glycoprotein is altered in a familial late-onset orthochromatic leukodystrophy 81
Myelin involvement in Niemann-Pick disease type A 81
Atypical histopathological changes in muscle biopsies from two patients with facioscapulohumeral muscular dystrophy 80
A new polymorphism, g119A>G, in the integrin alpha 7 (ITGA7) gene 80
[A comparison of histochemical features of some specific phosphatases in progressive muscular dystrophy, in neurogenic myopathies in man and in the denervated rat muscle (author's transl)] 79
Myelin-associated glycoprotein is altered in a familial orthochromatic leukodystrophy 79
Unusual clinical expression of dystrophinopathy in a female, mimicking a congenital myopathy. 78
A new method for myofibrillar Ca++-ATPase reaction based on the use of metachromatic dyes: its advantages in muscle fibre typing. 77
Osteomalacic myopathy in a case of diffuse nodular lipomatosis of the small bowel. 76
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophy. 76
Abnormal ubiquitination of axons in normally myelinated white matter in multiple sclerosis brain. 74
Congenital muscular dystrophy associated with familial junctional epidermolysis bullosa letalis. 73
[Recent acquisitions and prospects of research on Steinert's myotonic dystrophy. Histochemical and ultrastructural data] 72
Carrier detection of Duchenne muscular dystrophy through analysis of DNA from deciduous teeth of a dead affected child. 72
Body building and rhabdomyolysis. 71
Chondroitin, chondroitin 6-sulphate, chondroitin 4-sulphate and dermatan sulphate proteoglycans in normal and pathological human muscle. 69
Dystrophinopathy expressing as either cardiomyopathy or Becker dystrophy in the same family. 68
Myelin-associated glycoprotein is defective in a familial orthochromatic leukodystrophy 68
Cytochrome c oxidase and coenzyme Q in neuromuscular diseases: a histochemical study 67
Epidemiology of Duchenne muscular dystrophy in the province of Turin. 67
The significance of minimal alterations in muscle biopsy of Duchenne carriers. 67
Variable histological expression of dystrophinopathy in two females. 66
Familial progressive external ophthalmoplegia with multisystem abnormalities: 'new' features raising nosological problems. 64
Body building and myoglobinuria: report of three cases. 63
Myoglobinuria and carnitine palmityl transferase deficiency in father and son. 62
[Endo- and perimysial connective tissue in primary and secondary myopathies. Histochemical studies] 61
Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophy. 61
Myelin-associated glycoprotein is defective in a familail orthochromatic leukodystrophy 61
[Progressive muscular dystrophy of the Duchenne type. Epidemiology and strategy for prevention] 60
Glycogen storage disease type II diagnosed in a 74-year-old woman 60
[Individualization of carriers of Duchenne's muscular dystrophy by quantitative methods] 59
Familial autosomal recessive rigid spine syndrome with neurogenic facio-scapulo-peroneal muscle atrophy. 58
[Malignant intracranial and spinal lymphoma and sarcoma: review of our cases from the year 1960 to 1974] 58
Metachromatic dye-Ca++ATPase method in pathological muscle: a study of 382 muscle biopsies. 57
MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation. 54
Sporadic distal myopathy with early adult onset: study of muscle biopsies and muscle cell cultures. 53
Phenotypic clustering of lamin A/C mutations in neuromuscular patients. 53
Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult case. 52
Paraneoplastic opsoclonus-myoclonus associated with renal cell carcinoma and responsive to tumour ablation 52
Quantitative and qualitative alterations of dystrophin are expressed in muscle cell cultures of Xp21 muscular dystrophy patients (Duchenne and Becker type). 51
Motor neuron disease following poliomyelitis. Bioptic study of five cases. 50
Malattie neurologiche 50
Multidiscliplinary approach to cause and pathogenesis of an adult onset autosomal dominant orthochromatic leukodystrophy 47
Myopathy in a patient with chromosome 22q11 deletion. 45
Myoglobinuria: presentation of personal cases and review of the literature. 44
Quantitative analysis of quadriceps muscle biopsy. Results in 7 definite and 45 possible carriers of Duchenne muscular dystrophy. 43
Novel CLCN1 mutations with unique clinical and electrophysiological consequences. 42
SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy 41
Laminin and fibronectin distribution in normal and pathological human muscle. 40
Facioscapulohumeral muscular dystrophy: a multicenter study on hearing function. 39
Ineffectiveness of allopurinol in Duchenne muscular dystrophy. 39
Late onset and very mild course of Xp21 Becker type muscular dystrophy. 38
Facioscapulohumeral muscular dystrophy and occurrence of heart arrhythmia 38
Quantitative analysis of quadriceps muscle biopsy. Results in 30 healthy females. 37
Immunohistochemical localization of chondroitin sulfate in normal and pathological human muscle. 37
Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory disease. 37
Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency 35
Malattie mitocondriali 30
Totale 4.951
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Categoria #
all - tutte 15.802
article - articoli 0
book - libri 0
conference - conferenze 1.884
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 17.686
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020559 0 0 78 25 62 77 72 22 81 72 57 13
2020/2021537 56 11 65 24 52 21 61 9 113 46 29 50
2021/2022649 8 19 16 37 22 51 29 21 15 54 176 201
2022/20231.081 108 92 36 107 109 279 89 65 101 36 42 17
2023/2024340 59 82 13 19 18 49 10 6 4 7 13 60
2024/202553 1 31 21 0 0 0 0 0 0 0 0 0
Totale 4.951