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Results of search for 'au:"Del Giudice, E"', page 6 of 9
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Authors
Andria, G
Cirillo, G
Cutillo, S
Del Giudice, E
Delaunay, J
Grandone, A
Iolascon, A
Licenziati, M R
Maffeis, C
Manco, M
Miraglia Del Giudice, E
Miraglia del Giudice, E
Nobili, B
Perrone, L
Perrotta, S
Pinto, L
Romano, A
Santoro, N
del Giudice, E M
del Giudice, E Miraglia
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Adolescent
Adult
Child
Child, Preschool
Female
Humans
Infant
Italy
Male
Mutation
Obesity
Pedigree
Spherocytosis, Hereditary
blood
chemistry
complications
deficiency
diagnosis
genetics
metabolism
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English
g d
Italian
Your search returned 165 results.
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Results
101.
Sequential analysis of hepatitis B virus core promoter and precore regions in cancer survivor patients with chronic hepatitis B before, during and after interferon treatment.
[electronic resource]
by
Zampino, Rosa
Marrone, A
Cirillo, G
del Giudice, E Miraglia
Utili, R
Karayiannis, P
Liang, T J
Ruggiero, G
Producer:
20020801
In:
Journal of viral hepatitis
vol. 9
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102.
Dystrophinopathy in a young boy with Klinefelter's syndrome.
[electronic resource]
by
Santoro, L
Pastore, L
Rippa, P G
Orsini, A V
Del Giudice, E
Vita, G
Frisso, G
Salvatore, F
Producer:
19980521
In:
Muscle & nerve
vol. 21
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103.
Acute inflammatory demyelinating polyradiculoneuropathy associated with perforin-deficient familial haemophagocytic lymphohistiocytosis.
[electronic resource]
by
Del Giudice, E
Savoldi, G
Notarangelo, L D
Di Benedetto, L
Manganelli, F
Bruzzese, E
Romano, A
Santoro, L
Producer:
20030813
In:
Acta paediatrica (Oslo, Norway : 1992)
vol. 92
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104.
Spatial cognition in children. II. Visuospatial and constructional skills in developmental reading disability.
[electronic resource]
by
Del Giudice, E
Trojano, L
Fragassi, N A
Posteraro, S
Crisanti, A F
Tanzarella, P
Marino, A
Grossi, D
Producer:
20001222
In:
Brain & development
vol. 22
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105.
Early onset calpainopathy with normal non-functional calpain 3 level.
[electronic resource]
by
Lanzillo, R
Aurino, S
Fanin, M
Aguennoz, M
Vitale, F
Fiorillo, C
Del Giudice, E
Nigro, V
Santoro, L
Producer:
20060502
In:
Developmental medicine and child neurology
vol. 48
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106.
Flow-cytometric analysis of erythrocytes and reticulocytes in congenital dyserythropoietic anaemia type II (CDA II): value in differential diagnosis with hereditary spherocytosis.
[electronic resource]
by
Danise, P
Amendola, G
Nobili, B
Perrotta, S
Miraglia Del Giudice, E
Matarese, S M
Iolascon, A
Brugnara, C
Producer:
20010920
In:
Clinical and laboratory haematology
vol. 23
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107.
Increased membrane-protein methylation in hereditary spherocytosis. A marker of cytoskeletal disarray.
[electronic resource]
by
Ingrosso, D
D'Angelo, S
Perna, A F
Iolascon, A
Miraglia del Giudice, E
Perrotta, S
Zappia, V
Galletti, P
Producer:
19950602
In:
European journal of biochemistry
vol. 228
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108.
Decreased band 3 anion transport activity and band 3 clusterization in congenital dyserythropoietic anemia type II.
[electronic resource]
by
De Franceschi, L
Turrini, F
del Giudice, E M
Perrotta, S
Olivieri, O
Corrocher, R
Mannu, F
Iolascon, A
Producer:
19980818
In:
Experimental hematology
vol. 26
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109.
Molecular screening of the ghrelin gene in Italian obese children: the Leu72Met variant is associated with an earlier onset of obesity.
[electronic resource]
by
Miraglia del Giudice, E
Santoro, N
Cirillo, G
Raimondo, P
Grandone, A
D'Aniello, A
Di Nardo, M
Perrone, L
Producer:
20040429
In:
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity
vol. 28
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110.
Efficacy of very-low-dose betamethasone on neurological symptoms in ataxia-telangiectasia.
[electronic resource]
by
Broccoletti, T
Del Giudice, E
Cirillo, E
Vigliano, I
Giardino, G
Ginocchio, V M
Bruscoli, S
Riccardi, C
Pignata, C
Producer:
20110804
In:
European journal of neurology
vol. 18
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111.
Analysis of N-ras gene mutations in medulloblastomas by polymerase chain reaction and oligonucleotide probes in formalin-fixed, paraffin-embedded tissues.
[electronic resource]
by
Iolascon, A
Lania, A
Badiali, M
Pession, A
Saglio, G
Giangaspero, F
Miraglia del Giudice, E
Perrotta, S
Cutillo, S
Producer:
19910726
In:
Medical and pediatric oncology
vol. 19
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112.
Weight loss in obese children carrying the proopiomelanocortin R236G variant.
[electronic resource]
by
Santoro, N
Perrone, L
Cirillo, G
Raimondo, P
Amato, A
Coppola, F
Santarpia, M
D'Aniello, A
Miraglia Del Giudice, E
Producer:
20060609
In:
Journal of endocrinological investigation
vol. 29
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113.
Severe poikilocytosis associated with a de novo alpha 28 Arg-->Cys mutation in spectrin.
[electronic resource]
by
Lorenzo, F
Miraglia del Giudice, E
Alloisio, N
Morle, L
Forissier, A
Perrotta, S
Sciarratta, G
Iolascon, A
Delaunay, J
Producer:
19930324
In:
British journal of haematology
vol. 83
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114.
Low frequency of melanocortin-4 receptor (MC4R) mutations in a Mediterranean population with early-onset obesity.
[electronic resource]
by
Miraglia Del Giudice, E
Cirillo, G
Nigro, V
Santoro, N
D'Urso, L
Raimondo, P
Cozzolino, D
Scafato, D
Perrone, L
Producer:
20020624
In:
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity
vol. 26
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115.
A saturated N-acylethanolamine other than N-palmitoyl ethanolamine with anti-inflammatory properties: a neglected story...
[electronic resource]
by
Dalle Carbonare, M
Del Giudice, E
Stecca, A
Colavito, D
Fabris, M
D'Arrigo, A
Bernardini, D
Dam, M
Leon, A
Producer:
20080718
In:
Journal of neuroendocrinology
vol. 20 Suppl 1
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116.
Gastrointestinal manifestations in children with cerebral palsy.
[electronic resource]
by
Del Giudice, E
Staiano, A
Capano, G
Romano, A
Florimonte, L
Miele, E
Ciarla, C
Campanozzi, A
Crisanti, A F
Producer:
19990901
In:
Brain & development
vol. 21
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117.
Ankyrin Napoli: a de novo deletional frameshift mutation in exon 16 of ankyrin gene (ANK1) associated with spherocytosis.
[electronic resource]
by
del Giudice, E M
Hayette, S
Bozon, M
Perrotta, S
Alloisio, N
Vallier, A
Iolascon, A
Delaunay, J
Morlé, L
Producer:
19960912
In:
British journal of haematology
vol. 93
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118.
Smith Lemli-Opitz syndrome: a contribution to the delineation of a cognitive/behavioral phenotype.
[electronic resource]
by
De Clemente, V
Vitiello, G
Imperati, F
Romano, A
Parente, I
Rosa, M
Pascarella, A
Parenti, G
Del Giudice, E
Producer:
20130708
In:
Minerva pediatrica
vol. 65
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119.
Cytoskeletal behaviour in spectrin and in band 3 deficient spherocytic red cells: evidence for differentiated splenic conditioning role.
[electronic resource]
by
Ingrosso, D
D'Angelo, S
Perrotta, S
d'Urzo, G
Iolascon, A
Perna, A F
Galletti, P
Zappia, V
Miraglia del Giudice, E
Producer:
19960531
In:
British journal of haematology
vol. 93
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120.
Hereditary spherocytosis (HS) due to loss of anion exchange transporter.
[electronic resource]
by
Iolascon, A
Miraglia del Giudice, E
Perrotta, S
Pinto, L
Fiorelli, G
Cappellini, D M
Vasseur, C
Bursaux, E
Cutillo, S
Producer:
19930325
In:
Haematologica
vol. 77
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