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Results of search for 'au:"Papi, L"', page 1 of 3
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Authors
Ammannati, F
Baglioni, S
Ballestra, A M
Baser, M E
Bigozzi, U
Chiriatti, G
Contini, C
D'Angelo, T
De Vitis, L R
Filice, M
Gardner, E
Gistri, R
Giustarini, C
Guazzelli, R
L'Abbate, A
Maseri, A
Mennonna, P
Montali, E
Papi, L
Vitelli, F
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Base Sequence
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Chromosome Deletion
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 22
Coronary Disease
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Genes, Neurofibromatosis 2
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Meningeal Neoplasms
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1.
[Evaluation of the vagal components in disturbances of atrio-ventricular conduction and in bradycardia].
[electronic resource]
by
Papi, L
Maseri, A
Producer:
19720712
In:
Bollettino della Societa italiana di cardiologia
vol. 16
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2.
Dinucleotide repeat polymorphism at the RBP3 locus in chromosome band 10q11.2.
[electronic resource]
by
Papi, L
Tunnacliffe, A
Ponder, B A
Producer:
19930607
In:
Human molecular genetics
vol. 1
Online resources:
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3.
[Femoral compression neuropathy caused by spontaneous hematoma during heparin therapy: description of a case].
[electronic resource]
by
Papi, L
Nannini, E
Moroni, A
Iacopetti, L
Producer:
19890505
In:
Giornale italiano di cardiologia
vol. 18
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4.
[Hypertensive crisis during E.P.H. gestosis treated with sublingual nifedipine. Report of a case].
[electronic resource]
by
Papi, L
Giustarini, C
Filice, M
Ballestra, A M
Producer:
19860220
In:
Minerva cardioangiologica
vol. 33
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5.
[The hemisectorial role of the vagus nerve in migratory sinus arrhythmia with atrioventricular conduction disorder].
[electronic resource]
by
Papi, L
Tomei, G
Ballestra, A M
Filice, M
Producer:
19821221
In:
Minerva cardioangiologica
vol. 30
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6.
A new polymorphism in the ret protooncogene (RET).
[electronic resource]
by
Mulligan, L M
Gardner, E
Papi, L
Ponder, B A
Producer:
19911202
In:
Nucleic acids research
vol. 19
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7.
[Evolution of acute atrioventricular conduction disorders in acute infarct].
[electronic resource]
by
Contini, C
Papi, L
D'Angelo, T
Leone, A
Maseri, A
Producer:
19760520
In:
Bollettino della Societa italiana di cardiologia
vol. 17
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8.
Cutaneous foetal injuries related to amniocentesis.
[electronic resource]
by
Papi, L
Farusi, F
Teti, G
Dini, V
Romanelli, M
Producer:
20140107
In:
Journal of wound care
vol. 22
Online resources:
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9.
[Sublingual nifedipine in hypertensive crises].
[electronic resource]
by
Papi, L
Ballestra, A M
Tomei, G
Filice, M
Giustarini, C
Producer:
19830324
In:
Bollettino della Societa italiana di cardiologia
vol. 26
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10.
[Evaluation of the efficacy of indapamide in the treatment of essential arterial hypertension].
[electronic resource]
by
Papi, L
Ballestra, A M
Tomei, G
Filice, M
Giustarini, C
Producer:
19830324
In:
Bollettino della Societa italiana di cardiologia
vol. 26
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11.
[Clinical and angiographic correlations in coronary insufficiency].
[electronic resource]
by
Maseri, A
L'Abbate, A
Contini, C
Pesola, A
Papi, L
D'Angelo, T
Producer:
19730406
In:
Bollettino della Societa italiana di cardiologia
vol. 17
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12.
[Pulmonary venous congestion: pressure and volume of pulmonary blood in acute myocardial infarct].
[electronic resource]
by
Maseri, A
Pesola, A
Contini, C
L'Abbate, A
Papi, L
D'Angelo, T
Producer:
19741118
In:
Bollettino della Societa italiana di cardiologia
vol. 17
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13.
Prognostic significance of microsatellite instability in sporadic mucinous colorectal cancers.
[electronic resource]
by
Messerini, L
Ciantelli, M
Baglioni, S
Palomba, A
Zampi, G
Papi, L
Producer:
19990701
In:
Human pathology
vol. 30
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14.
[Clinical use of mazindol in the treatment of essential obesity].
[electronic resource]
by
Guazzelli, R
Piazzini, M
Conti, C
Papi, L
Strazzulla, G
Matassi, L
Producer:
19870707
In:
La Clinica terapeutica
vol. 120
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15.
Neurofibromatosis type 2 attributable to gonosomal mosaicism in a clinically normal mother, and identification of seven novel mutations in the NF2 gene.
[electronic resource]
by
Sestini, R
Vivarelli, R
Balestri, P
Ammannati, F
Montali, E
Papi, L
Producer:
20010104
In:
Human genetics
vol. 107
Online resources:
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16.
An Italian family affected by Nasu-Hakola disease with a novel genetic mutation in the TREM2 gene.
[electronic resource]
by
Soragna, D
Papi, L
Ratti, M T
Sestini, R
Tupler, R
Montalbetti, L
Producer:
20030708
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 74
Online resources:
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17.
Cytogenetic studies in sporadic and multiple endocrine neoplasia type 1-associated pituitary adenomas.
[electronic resource]
by
Papi, L
Baldassarri, G
Montali, E
Bigozzi, U
Ammannati, F
Brandi, M L
Producer:
19930916
In:
Genes, chromosomes & cancer
vol. 7
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18.
Evidence for a human mitotic mutant with pleiotropic effect.
[electronic resource]
by
Papi, L
Montali, E
Marconi, G
Guazzelli, R
Bigozzi, U
Maraschio, P
Zuffardi, O
Producer:
19900124
In:
Annals of human genetics
vol. 53
Online resources:
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19.
True hermaphroditism: a new case with complex mosaicism.
[electronic resource]
by
Borghi, A
Papi, L
Bigozzi, U
Biagioni, M
Taddei, G L
Natali, A
Maiello, M
Producer:
19901220
In:
Genetic counseling (Geneva, Switzerland)
vol. 1
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20.
Somatic mutations in the neurofibromatosis type 2 gene in sporadic meningiomas.
[electronic resource]
by
Papi, L
De Vitis, L R
Vitelli, F
Ammannati, F
Mennonna, P
Montali, E
Bigozzi, U
Producer:
19950324
In:
Human genetics
vol. 95
Online resources:
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