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Gaucher's disease with Parkinson's disease: clinical and pathological aspects. [electronic resource] by
- Bembi, B
- Zambito Marsala, S
- Sidransky, E
- Ciana, G
- Carrozzi, M
- Zorzon, M
- Martini, C
- Gioulis, M
- Pittis, M G
- Capus, L
Producer: 20040129
In:
Neurology vol. 61
Availability: No items available.
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Two novel POLG mutations causing hepatic mitochondrial DNA depletion with recurrent hypoketotic hypoglycaemia and fatal liver dysfunction. [electronic resource] by
- Bortot, B
- Barbi, E
- Biffi, S
- Lunazzi, G
- Bussani, R
- Burlina, A
- Norbedo, S
- Ventura, A
- Carrozzi, M
- Severini, G M
Producer: 20090826
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
Availability: No items available.
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Endozepine stupor in children. [electronic resource] by
- Soriani, S
- Carrozzi, M
- De Carlo, L
- Plazzi, G
- Provini, F
- Rothstein, J D
- Tinuper, P
- Bouquet, F
- Lugaresi, E
- Montagna, P
Producer: 19971209
In:
Cephalalgia : an international journal of headache vol. 17
Availability: No items available.
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Carbohydrate-deficient glycoprotein syndromes: the Italian experience. [electronic resource] by
- Di Rocco, M
- Barone, R
- Adami, A
- Burlina, A
- Carrozzi, M
- Dionisi-Vici, C
- Gatti, R
- Iannetti, P
- Parini, R
- Raucci, U
- Roccella, M
- Spada, M
- Fiumara, A
Producer: 20001116
In:
Journal of inherited metabolic disease vol. 23
Availability: No items available.
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A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation. [electronic resource] by
- Barone, Rita
- Carrozzi, M
- Parini, R
- Battini, R
- Martinelli, D
- Elia, M
- Spada, M
- Lilliu, F
- Ciana, G
- Burlina, A
- Leuzzi, V
- Leoni, M
- Sturiale, L
- Matthijs, G
- Jaeken, J
- Di Rocco, M
- Garozzo, D
- Fiumara, A
Producer: 20160404
In:
Journal of neurology vol. 262
Availability: No items available.
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