Macciotta A - Search Results

1

Homozygous non-deletion alpha 2 globin gene mutation (initiation codon mutation): clinical and haematological phenotype.

Galanello R, Monne MI, Paderi L, Paglietti E, Atzori G, Addis M, Limongelli O, Macciotta A, Cao A. Galanello R, et al. Among authors: macciotta a. Br J Haematol. 1991 Sep;79(1):117-9. doi: 10.1111/j.1365-2141.1991.tb08018.x. Br J Haematol. 1991. PMID: 1911369 No abstract available.

2

Alpha-thalassemia in premature newborns.

Maccioni L, Galanello R, Ruggeri R, Puddu R, Rosatelli D, Marras A, Chiappe S, Macciotta A, Cao A. Maccioni L, et al. Among authors: macciotta a. Pediatr Res. 1986 Nov;20(11):1077-81. doi: 10.1203/00006450-198611000-00003. Pediatr Res. 1986. PMID: 3797101

3

[The isoenzymes of lactate dehydrogenase and glutamic-oxalacetic transaminase in fetal and adult muscle and muscle of subjects affected by the Duchenne type of progressive muscular dystrophy].

Mannucci PM, Idèo G, Cao A, Macciotta A. Mannucci PM, et al. Among authors: macciotta a. Rass Med Sarda. 1965 May-Jun;68(3):287-99. Rass Med Sarda. 1965. PMID: 5844059 Italian. No abstract available.

4

[The isoenzymes of lactate dehydrogenase (LDH), glutamic-oxalacetic transaminase (GOT) and malate dehydrogenase(MDH) in subjects with fetal muscular dystrophy and spinal amyotrophy of the Werdnig-Hoffman type].

Cao A, Macciotta A, Idéo G, Munnucci PM. Cao A, et al. Among authors: macciotta a. Boll Soc Ital Biol Sper. 1966 Jun 30;42(12):709-13. Boll Soc Ital Biol Sper. 1966. PMID: 6008535 Italian. No abstract available.

5

Chromatographic and electrophoretic pattern of lactate and malate dehydrogenase in normal human adult and foetal muscle and in muscle of patients affected by Duchenne muscular dystrophy.

Cao A, Macciotta A, Fiorelli G, Mannucci PM, Idéo G. Cao A, et al. Among authors: macciotta a. Enzymol Biol Clin (Basel). 1966;7(3):156-66. doi: 10.1159/000457301. Enzymol Biol Clin (Basel). 1966. PMID: 5965867 No abstract available.

6

Epidermolysis bullosa and amniotic bands.

Marras A, Dessì C, Macciotta A. Marras A, et al. Among authors: macciotta a. Am J Med Genet. 1984 Dec;19(4):815-7. doi: 10.1002/ajmg.1320190423. Am J Med Genet. 1984. PMID: 6517104 No abstract available.

7

[Pathogenesis of atresia of the pylorus in patients with epidermolysis bullosa].

Marras A, Dessì C, Macciotta A. Marras A, et al. Among authors: macciotta a. Pediatr Med Chir. 1984 Nov-Dec;6(6):839-42. Pediatr Med Chir. 1984. PMID: 6545599 Italian.

8

Oligohydramnios and extrarenal abnormalities in Potter syndrome.

Marras A, Mereu G, Dessi C, Macciotta A. Marras A, et al. Among authors: macciotta a. J Pediatr. 1983 Apr;102(4):597-8. doi: 10.1016/s0022-3476(83)80196-6. J Pediatr. 1983. PMID: 6834196 No abstract available.

9

Multimorbidity and COVID-19 Outcomes in the Emergency Department: Is the Association Mediated by the Severity of the Condition at Admission?

Catalano A, Sacerdote C, Alvich M, Macciotta A, Milani L, Destefanis C, Gebru KT, Sodano B, Padroni L, Giraudo MT, Ciccone G, Pagano E, Boccuzzi A, Caramello V, Ricceri F. Catalano A, et al. Among authors: macciotta a. J Clin Med. 2024 Nov 26;13(23):7182. doi: 10.3390/jcm13237182. J Clin Med. 2024. PMID: 39685641 Free PMC article.

10

Examining causal relationships between educational attainment and type 2 diabetes using genetic analysis: findings from the EPIC-InterAct study through Mendelian randomisation.

Macciotta A, Sacerdote C, Giachino C, Di Girolamo C, Franco M, van der Schouw YT, Zamora-Ros R, Weiderpass E, Domenighetti C, Elbaz A, Truong T, Agnoli C, Bendinelli B, Panico S, Vineis P, Christakoudi S, Schulze MB, Katzke V, Bajracharya R, Dahm CC, Dalton SO, Colorado-Yohar SM, Moreno-Iribas C, Etxezarreta PA, Sanchez MJ, Forouhi NG, Wareham N, Ricceri F. Macciotta A, et al. J Epidemiol Community Health. 2024 Dec 10:jech-2024-222734. doi: 10.1136/jech-2024-222734. Online ahead of print. J Epidemiol Community Health. 2024. PMID: 39658133

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