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Results of search for 'au:"del Giudice, E"', page 5 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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Child
Child, Preschool
Female
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Italy
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Spherocytosis, Hereditary
blood
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complications
deficiency
diagnosis
genetics
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Italian
Your search returned 165 results.
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81.
[Bone changes in homocystinuria in childhood].
[electronic resource]
by
Tamburrini, O
Bartolomeo-De Iuri, A
Andria, G
Strisciuglio, P
Del Giudice, E
Palescandolo, P
Sartorio, R
Producer:
19860228
In:
La Radiologia medica
vol. 70
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82.
Effect of body mass index reduction on serum hepcidin levels and iron status in obese children.
[electronic resource]
by
Amato, A
Santoro, N
Calabrò, P
Grandone, A
Swinkels, D W
Perrone, L
del Giudice, E Miraglia
Producer:
20110418
In:
International journal of obesity (2005)
vol. 34
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83.
P16INK4A gene homozygous deletions in human acute leukaemias with alterations of chromosome 9.
[electronic resource]
by
Faienza, M F
della Ragione, F
Basso, G
Coppola, B
Miraglia del Giudice, E
Schettini, F
Iolascon, A
Producer:
19960729
In:
British journal of haematology
vol. 93
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84.
p16INK4 gene deletions in childhood acute lymphoblastic leukemias.
[electronic resource]
by
Iolasceon, A
Del Giudice, E M
Perrotta, S
Russo, G L
Oliva, A
Mercurio, C
Della Ragione, F
Producer:
19960221
In:
Leukemia research
vol. 19
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85.
Brain migration disorder and T-cell activation deficiency associated with abnormal signaling through TCR/CD3 complex and hyperactivity of Fyn tyrosine kinase.
[electronic resource]
by
Del Giudice, E
Gaetaniello, L
Matrecano, E
Cosentini, E
Ursini, M V
Racioppi, L
Arrigo, G
Pignata, C
Producer:
20010405
In:
Neuropediatrics
vol. 31
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86.
Low-protein diet and progression of retinal degeneration in gyrate atrophy of the choroid and retina: a twenty-six-year follow-up.
[electronic resource]
by
Santinelli, R
Costagliola, C
Tolone, C
D'Aloia, A
D'Avanzo, A
Prisco, F
Perrone, L
del Giudice, E Miraglia
Producer:
20041230
In:
Journal of inherited metabolic disease
vol. 27
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87.
The insulin gene variable number of tandemrepeats (INS VNTR) genotype and sleep disordered breathing in childhood obesity.
[electronic resource]
by
Carotenuto, M
Santoro, N
Grandone, A
Santoro, E
Pascotto, C
Pascotto, A
Perrone, L
del Giudice, E Miraglia
Producer:
20100225
In:
Journal of endocrinological investigation
vol. 32
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88.
Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome.
[electronic resource]
by
Iolascon, A
Faienza, M F
Giordani, L
Perrotta, S
Ruggiu, G
Meloni, G F
del Giudice, E M
Producer:
19990623
In:
European journal of haematology
vol. 62
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89.
Hyperekplexia caused by dominant-negative suppression of glyra1 function.
[electronic resource]
by
Bellini, G
Miceli, F
Mangano, S
Miraglia del Giudice, E
Coppola, G
Barbagallo, A
Taglialatela, M
Pascotto, A
Producer:
20070712
In:
Neurology
vol. 68
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90.
Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74).
[electronic resource]
by
Perrotta, S
Miraglia del Giudice, E
Alloisio, N
Sciarratta, G
Pinto, L
Delaunay, J
Cutillo, S
Iolascon, A
Producer:
19940627
In:
Blood
vol. 83
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91.
Molecular screening of the proopiomelanocortin (POMC ) gene in Italian obese children: report of three new mutations.
[electronic resource]
by
Miraglia del Giudice, E
Cirillo, G
Santoro, N
D'Urso, L
Carbone, M T
Di Toro, R
Perrone, L
Producer:
20011205
In:
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity
vol. 25
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92.
Reversible erythrocyte skeleton destabilization is modulated by beta-spectrin phosphorylation in childhood leukemia.
[electronic resource]
by
Perrotta, S
del Giudice, E M
Iolascon, A
De Vivo, M
Di Pinto, D
Cutillo, S
Nobili, B
Producer:
20010329
In:
Leukemia
vol. 15
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93.
Steroid-induced improvement of neurological signs in ataxia-telangiectasia patients.
[electronic resource]
by
Broccoletti, T
Del Giudice, E
Amorosi, S
Russo, I
Di Bonito, M
Imperati, F
Romano, A
Pignata, C
Producer:
20080403
In:
European journal of neurology
vol. 15
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94.
Mild Wolf-Hirschhorn phenotype and partial GH deficiency in a patient with a 4p terminal deletion.
[electronic resource]
by
Titomanlio, L
Romano, A
Conti, A
Genesio, R
Salerno, M
De Brasi, D
Nitsch, L
Del Giudice, E
Producer:
20050204
In:
American journal of medical genetics. Part A
vol. 127A
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95.
Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search.
[electronic resource]
by
Gasparini, P
Miraglia del Giudice, E
Delaunay, J
Totaro, A
Granatiero, M
Melchionda, S
Zelante, L
Iolascon, A
Producer:
19971212
In:
American journal of human genetics
vol. 61
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96.
Dynamics of the ion cyclotron resonance effect on amino acids adsorbed at the interfaces.
[electronic resource]
by
Comisso, N
Del Giudice, E
De Ninno, A
Fleischmann, M
Giuliani, L
Mengoli, G
Merlo, F
Talpo, G
Producer:
20060120
In:
Bioelectromagnetics
vol. 27
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97.
A common CTLA4 polymorphism confers susceptibility to autoimmune thyroid disease in celiac children.
[electronic resource]
by
Tolone, C
Cirillo, G
Papparella, A
Tolone, S
Santoro, N
Grandone, A
Perrone, L
del Giudice, E Miraglia
Producer:
20090805
In:
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver
vol. 41
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98.
Do MYO9B genetic variants predispose to coeliac disease? An association study in a cohort of South Italian children.
[electronic resource]
by
Cirillo, G
Di Domenico, M R
Corsi, I
Gagliardo, T
Del Giudice, E M
Perrone, L
Tolone, C
Producer:
20070501
In:
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver
vol. 39
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99.
Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African origin.
[electronic resource]
by
del Giudice, E M
Ducluzeau, M T
Alloisio, N
Wilmotte, R
Delaunay, J
Perrotta, S
Cutillo, S
Iolascon, A
Producer:
19920825
In:
Human genetics
vol. 89
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100.
Frequent de novo mutations of the ANK1 gene mimic a recessive mode of transmission in hereditary spherocytosis: three new ANK1 variants: ankyrins Bari, Napoli II and Anzio.
[electronic resource]
by
Randon, J
Miraglia del Giudice, E
Bozon, M
Perrotta, S
De Vivo, M
Iolascon, A
Delaunay, J
Morle, L
Producer:
19970417
In:
British journal of haematology
vol. 96
Online resources:
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