CINECA IRIS Institutional Research Information System

PALMUCCI, Laura Maria
 Distribuzione geografica
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Continente #
NA - Nord America 2.012
EU - Europa 1.984
AS - Asia 632
AF - Africa 17
Continente sconosciuto - Info sul continente non disponibili 5
SA - Sud America 3
OC - Oceania 2
Totale 4.655
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Nazione #
US - Stati Uniti d'America 1.945
CN - Cina 421
UA - Ucraina 327
SE - Svezia 302
IE - Irlanda 253
DE - Germania 249
FR - Francia 161
IT - Italia 156
FI - Finlandia 149
KR - Corea 145
AT - Austria 144
GB - Regno Unito 136
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
SG - Singapore 1
SI - Slovenia 1
UY - Uruguay 1
Totale 4.655
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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
Houston 64
Medford 64
Ashburn 60
Milan 58
Boston 50
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
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
Pune 4
Seattle 4
Turin 4
Bologna 3
Changsha 3
Cincinnati 3
Como 3
Craiova 3
Guangzhou 3
Hebei 3
Los Angeles 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
Rome 2
Ruma 2
Shanghai 2
Stavanger 2
Tappahannock 2
University Park 2
Alicante 1
Ardabil 1
Bitetto 1
Borgomanero 1
Bottmingen 1
Carcavelos 1
Charlotte 1
Chengdu 1
Chester 1
Châtillon 1
Englewood 1
Totale 2.633
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Nome #
Chinese red rice depletes muscle coenzyme Q10 and maintains muscle damage after discontinuation of statin treatment 150
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. 120
Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuria. 117
Muscular involvement in Whipple's disease with gastrointestinal sparing 103
A defective L_MAG (large myelin-associated glycoprotein) is responsible for an adult-onset autosomal dominant orthochromatic leukodystrophy 102
Central core disease: histochemical and ultrastructural study of muscle biopsies of father and daughter. 95
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency 91
Analysis of some factors effecting survival in malignant gliomas. 90
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. 86
Spongiform encephalopathy in addicts inhaling pre-heated heroin. 85
La distrofia muscolare oculo-faringea: caratteristiche cliniche e genetiche 83
Sporadic ulcerative mutilating acropathy with imbalance of free amino acids in the cerebrospinal fluid. 82
Adult onset nemaline myopathy: a distinct nosologic entity? 82
Myelin involvement in Niemann-Pick disease type A 81
Myelin-associated glycoprotein is altered in a familial late-onset orthochromatic leukodystrophy 80
Atypical histopathological changes in muscle biopsies from two patients with facioscapulohumeral muscular dystrophy 80
Systematic use of dystrophin testing in muscle biopsies: results in 201 cases. 80
Clinical spectrum of McArdle disease: three cases with unusual expression. 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
Absence of dystrophin in two patients with Becker type Xp21 muscular dystrophy. 79
A new polymorphism, g119A>G, in the integrin alpha 7 (ITGA7) gene 78
Unusual clinical expression of dystrophinopathy in a female, mimicking a congenital myopathy. 77
Myelin-associated glycoprotein is altered in a familial orthochromatic leukodystrophy 77
A new method for myofibrillar Ca++-ATPase reaction based on the use of metachromatic dyes: its advantages in muscle fibre typing. 76
Osteomalacic myopathy in a case of diffuse nodular lipomatosis of the small bowel. 75
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophy. 75
Abnormal ubiquitination of axons in normally myelinated white matter in multiple sclerosis brain. 73
[Recent acquisitions and prospects of research on Steinert's myotonic dystrophy. Histochemical and ultrastructural data] 70
Carrier detection of Duchenne muscular dystrophy through analysis of DNA from deciduous teeth of a dead affected child. 70
Body building and rhabdomyolysis. 70
Chondroitin, chondroitin 6-sulphate, chondroitin 4-sulphate and dermatan sulphate proteoglycans in normal and pathological human muscle. 69
Congenital muscular dystrophy associated with familial junctional epidermolysis bullosa letalis. 69
Dystrophinopathy expressing as either cardiomyopathy or Becker dystrophy in the same family. 67
Cytochrome c oxidase and coenzyme Q in neuromuscular diseases: a histochemical study 66
The significance of minimal alterations in muscle biopsy of Duchenne carriers. 66
Variable histological expression of dystrophinopathy in two females. 65
Myelin-associated glycoprotein is defective in a familial orthochromatic leukodystrophy 65
Familial progressive external ophthalmoplegia with multisystem abnormalities: 'new' features raising nosological problems. 63
Epidemiology of Duchenne muscular dystrophy in the province of Turin. 63
Myoglobinuria and carnitine palmityl transferase deficiency in father and son. 61
[Endo- and perimysial connective tissue in primary and secondary myopathies. Histochemical studies] 60
Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophy. 60
Glycogen storage disease type II diagnosed in a 74-year-old woman 59
Myelin-associated glycoprotein is defective in a familail orthochromatic leukodystrophy 59
Body building and myoglobinuria: report of three cases. 58
[Individualization of carriers of Duchenne's muscular dystrophy by quantitative methods] 57
Familial autosomal recessive rigid spine syndrome with neurogenic facio-scapulo-peroneal muscle atrophy. 57
[Malignant intracranial and spinal lymphoma and sarcoma: review of our cases from the year 1960 to 1974] 57
[Progressive muscular dystrophy of the Duchenne type. Epidemiology and strategy for prevention] 56
Metachromatic dye-Ca++ATPase method in pathological muscle: a study of 382 muscle biopsies. 56
Sporadic distal myopathy with early adult onset: study of muscle biopsies and muscle cell cultures. 52
Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult case. 51
MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation. 51
Paraneoplastic opsoclonus-myoclonus associated with renal cell carcinoma and responsive to tumour ablation 51
Phenotypic clustering of lamin A/C mutations in neuromuscular patients. 50
Quantitative and qualitative alterations of dystrophin are expressed in muscle cell cultures of Xp21 muscular dystrophy patients (Duchenne and Becker type). 50
Malattie neurologiche 49
Motor neuron disease following poliomyelitis. Bioptic study of five cases. 48
Myopathy in a patient with chromosome 22q11 deletion. 44
Quantitative analysis of quadriceps muscle biopsy. Results in 7 definite and 45 possible carriers of Duchenne muscular dystrophy. 42
Myoglobinuria: presentation of personal cases and review of the literature. 42
Novel CLCN1 mutations with unique clinical and electrophysiological consequences. 41
Multidiscliplinary approach to cause and pathogenesis of an adult onset autosomal dominant orthochromatic leukodystrophy 41
Laminin and fibronectin distribution in normal and pathological human muscle. 39
Ineffectiveness of allopurinol in Duchenne muscular dystrophy. 38
SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy 38
Late onset and very mild course of Xp21 Becker type muscular dystrophy. 37
Facioscapulohumeral muscular dystrophy and occurrence of heart arrhythmia 37
Quantitative analysis of quadriceps muscle biopsy. Results in 30 healthy females. 36
Immunohistochemical localization of chondroitin sulfate in normal and pathological human muscle. 36
Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory disease. 36
Facioscapulohumeral muscular dystrophy: a multicenter study on hearing function. 35
Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency 32
Malattie mitocondriali 29
Totale 4.824
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Categoria #
all - tutte 13.641
article - articoli 0
book - libri 0
conference - conferenze 1.602
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 15.243
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019107 0 0 0 0 0 0 0 0 0 25 57 25
2019/2020609 17 33 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
2023/2024266 59 82 13 19 18 49 10 6 4 6 0 0
Totale 4.824