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Early signs of vascular disease in homocystinuria: a noninvasive study by ultrasound methods in eight families with cystathionine-beta-synthase deficiency. [electronic resource] by
- Rubba, P
- Faccenda, F
- Pauciullo, P
- Carbone, L
- Mancini, M
- Strisciuglio, P
- Carrozzo, R
- Sartorio, R
- del Giudice, E
- Andria, G
Producer: 19901204
In:
Metabolism: clinical and experimental vol. 39
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128.
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In ataxia-teleangiectasia betamethasone response is inversely correlated to cerebellar atrophy and directly to antioxidative capacity. [electronic resource] by
- Russo, I
- Cosentino, C
- Del Giudice, E
- Broccoletti, T
- Amorosi, S
- Cirillo, E
- Aloj, G
- Fusco, A
- Costanzo, V
- Pignata, C
Producer: 20090817
In:
European journal of neurology vol. 16
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The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulum. [electronic resource] by
- Alloisio, N
- Texier, P
- Denoroy, L
- Berger, C
- Miraglia del Giudice, E
- Perrotta, S
- Iolascon, A
- Gilsanz, F
- Berger, G
- Guichard, J
Producer: 19960716
In:
Blood vol. 87
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Gene symbol: MECP2. Disease: Rett syndrome. [electronic resource] by
- Conforti, F L
- Mazzei, R
- Patitucci, A
- Magariello, A
- Sprovieri, T
- Ungaro, C
- Gabriele, A L
- Muglia, M
- Del Giudice, E
- Quattrone, A
Producer: 20061207
In:
Human genetics vol. 119
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Glucose 6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia. [electronic resource] by
- Alfinito, F
- Calabro, V
- Cappellini, M D
- Fiorelli, G
- Filosa, S
- Iolascon, A
- Miraglia del Giudice, E
- Perrotta, S
- Migliorati, R
- Vallone, D
Producer: 19941207
In:
British journal of haematology vol. 87
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139.
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Association between cannabinoid receptor type 2 Q63R variant and oligo/polyarticular juvenile idiopathic arthritis. [electronic resource] by
- Bellini, G
- Olivieri, A N
- Grandone, A
- Alessio, M
- Gicchino, M F
- Nobili, B
- Perrone, L
- Maione, S
- del Giudice, E Miraglia
- Rossi, F
Producer: 20151008
In:
Scandinavian journal of rheumatology vol. 44
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140.
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Lack of red hair phenotype in a North-African obese child homozygous for a novel POMC null mutation: nonsense-mediated decay RNA evaluation and hair pigment chemical analysis. [electronic resource] by
- Cirillo, G
- Marini, R
- Ito, S
- Wakamatsu, K
- Scianguetta, S
- Bizzarri, C
- Romano, A
- Grandone, A
- Perrone, L
- Cappa, M
- Miraglia Del Giudice, E
Producer: 20130606
In:
The British journal of dermatology vol. 167
Availability: No items available.
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