Angelini C - Search Results

1

Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiency.

Martinuzzi A, Vergani L, Carrozzo R, Fanin M, Bartoloni L, Angelini C, Askanas V, Engel WK. Martinuzzi A, et al. Among authors: angelini c. J Clin Invest. 1993 Oct;92(4):1774-80. doi: 10.1172/JCI116766. J Clin Invest. 1993. PMID: 8408630 Free PMC article.

2

Carnitine deficiency: acute postpartum crisis.

Angelini C, Govoni E, Bragaglia MM, Vergani L. Angelini C, et al. Ann Neurol. 1978 Dec;4(6):558-61. doi: 10.1002/ana.410040616. Ann Neurol. 1978. PMID: 742856

3

Variability of the expression of muscle mitochondrial damage in ocular mitochondrial myopathy.

Siciliano G, Rossi B, Angelini C, Martinuzzi A, Carrozzo R, Bevilacqua G, Viacava P, Federico A, Fabrizi GM, Muratorio A. Siciliano G, et al. Among authors: angelini c. Neuromuscul Disord. 1992;2(5-6):397-404. doi: 10.1016/s0960-8966(06)80011-8. Neuromuscul Disord. 1992. PMID: 1300188

4

Correlation between clinical and molecular features in two MELAS families.

Martinuzzi A, Bartolomei L, Carrozzo R, Mostacciuolo M, Carbonin C, Toso V, Ciafaloni E, Shanske S, DiMauro S, Angelini C. Martinuzzi A, et al. Among authors: angelini c. J Neurol Sci. 1992 Dec;113(2):222-9. doi: 10.1016/0022-510x(92)90250-o. J Neurol Sci. 1992. PMID: 1487758

5

Clinical and biochemical aspects of carnitine deficiency and insufficiency: transport defects and inborn errors of beta-oxidation.

Angelini C, Vergani L, Martinuzzi A. Angelini C, et al. Crit Rev Clin Lab Sci. 1992;29(3-4):217-42. doi: 10.3109/10408369209114601. Crit Rev Clin Lab Sci. 1992. PMID: 1489518 Review.

6

Prevalence of dystrophin-positive fibers in 85 Duchenne muscular dystrophy patients.

Fanin M, Danieli GA, Vitiello L, Senter L, Angelini C. Fanin M, et al. Among authors: angelini c. Neuromuscul Disord. 1992;2(1):41-5. doi: 10.1016/0960-8966(92)90025-2. Neuromuscul Disord. 1992. PMID: 1525557

7

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts.

Chomyn A, Martinuzzi A, Yoneda M, Daga A, Hurko O, Johns D, Lai ST, Nonaka I, Angelini C, Attardi G. Chomyn A, et al. Among authors: angelini c. Proc Natl Acad Sci U S A. 1992 May 15;89(10):4221-5. doi: 10.1073/pnas.89.10.4221. Proc Natl Acad Sci U S A. 1992. PMID: 1584755 Free PMC article.

8

Echocardiographic and pulsed Doppler features in glycogen storage disease type II of the heart (Pompe's disease).

De Dominicis E, Finocchi G, Vincenzi M, Calvelli M, Ronconi G, Angelini C, Vergani L. De Dominicis E, et al. Among authors: angelini c. Acta Cardiol. 1991;46(1):107-14. Acta Cardiol. 1991. PMID: 1827699

9

Muscle carnitine deficiency in patients with severe peripheral vascular disease.

Brevetti G, Angelini C, Rosa M, Carrozzo R, Perna S, Corsi M, Matarazzo A, Marcialis A. Brevetti G, et al. Among authors: angelini c. Circulation. 1991 Oct;84(4):1490-5. doi: 10.1161/01.cir.84.4.1490. Circulation. 1991. PMID: 1914091

10

L-carnitine uptake in differentiating human cultured muscle.

Martinuzzi A, Vergani L, Rosa M, Angelini C. Martinuzzi A, et al. Among authors: angelini c. Biochim Biophys Acta. 1991 Nov 12;1095(3):217-22. doi: 10.1016/0167-4889(91)90102-4. Biochim Biophys Acta. 1991. PMID: 1958696

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