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Results of search for 'au:"Macciotta, A"'
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Authors
Addis, M
Altieri, M
Andria, C
Atzori, G
Batetta, B
CHIAPPE, F
CHIAPPE, S
Cao, A
Chiappe, S
Corrias, F
Dessi, C
Dessi, S
Dessì, C
Galanello, R
Idéo, G
MACCIOTTA, A
Macciotta, A
Mannucci, P M
Marras, A
Pani, P
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Topics
Adult
Aspartate Aminotransferases
Child
Chromatography
Female
Humans
Infant
Infant, Newborn
Isoenzymes
L-Lactate Dehydrogenase
Male
Muscles
Muscular Dystrophies
Phenotype
Pregnancy
analysis
blood
enzymology
genetics
metabolism
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Italian
Undetermined
Your search returned 19 results.
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1.
[Pediatric pathology and oral diseases (the pediatric viewpoint)].
[electronic resource]
by
Macciotta, A
Producer:
19790428
In:
Mondo ortodontico
vol. 3
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2.
[Possible relations between blood group incompatibility in ABO system and natural prezygotic selection].
[electronic resource]
by
Macciotta, A
Producer:
19710729
In:
La Pediatria
vol. 78
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3.
[Nipiopharmacology of steroid hormones].
[electronic resource]
by
Macciotta, A
Producer:
19691005
In:
Minerva nipiologica
vol. 17
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4.
[The action of the thymus on the metabolism of fatty acids and exudative diathesis syndromes of the infant].
[electronic resource]
by
MACCIOTTA, A
Producer:
20030501
In:
Rivista di clinica pediatrica
vol. 51
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5.
[Rare cardiac abnormality in an infant; clinico-functional and anatomico-histological research].
[electronic resource]
by
SCHLICH, G
MACCIOTTA, A
Producer:
20030501
In:
Archivio italiano di anatomia e istologia patologica
vol. 30
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6.
Epidermolysis bullosa and amniotic bands.
[electronic resource]
by
Marras, A
Dessì, C
Macciotta, A
Producer:
19850205
In:
American journal of medical genetics
vol. 19
Online resources:
Available from publisher's website
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7.
[Pathogenesis of atresia of the pylorus in patients with epidermolysis bullosa].
[electronic resource]
by
Marras, A
Dessì, C
Macciotta, A
Producer:
19860320
In:
La Pediatria medica e chirurgica : Medical and surgical pediatrics
vol. 6
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8.
[The newborn infant with very low birth weight. Etiopathogenetic factors; clinico-metabolic characteristics; criteria for medical care].
[electronic resource]
by
Macciotta, A
Chiappe, S
Diana, G
Producer:
19750621
In:
Minerva pediatrica
vol. 26
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9.
[APPLICATION OF THE DAHLBERT METHOD (COMPARISON OF VARIABILITY BETWEEN SERIES OF MZ AND DZ TWIN PAIRS) TO THE STUDY OF SOMATIC VALUE IN THE NEWBORN].
[electronic resource]
by
CHIAPPE, F
MACCIOTTA, A
CHIAPPE, S
Producer:
19961201
In:
Minerva nipiologica
vol. 15
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10.
[Studies on the degree of sex development in a group of adolescents of southern Sardinia].
[electronic resource]
by
Macciotta, A
Marini Carta, A
Corrias, F
Producer:
19710225
In:
Minerva pediatrica
vol. 22
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11.
[ON THE PROBLEM OF SO-CALLED "LAMELLAR EXFOLIATION OF THE NEWBORN" OR "COLLODION SKIN"].
[electronic resource]
by
LEONE, A
MACCIOTTA, A
FERRELI, A
CHIAPPE, F
Producer:
19961201
In:
Rassegna medica sarda
vol. 66
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12.
Oligohydramnios and extrarenal abnormalities in Potter syndrome.
[electronic resource]
by
Marras, A
Mereu, G
Dessi, C
Macciotta, A
Producer:
19830505
In:
The Journal of pediatrics
vol. 102
Online resources:
Available from publisher's website
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13.
[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].
[electronic resource]
by
Cao, A
Macciotta, A
Idéo, G
Munnucci, P M
Producer:
19670926
In:
Bollettino della Societa italiana di biologia sperimentale
vol. 42
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14.
[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].
[electronic resource]
by
Mannucci, P M
Idèo, G
Cao, A
Macciotta, A
Producer:
19660203
In:
Rassegna medica sarda
vol. 68
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15.
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.
[electronic resource]
by
Cao, A
Macciotta, A
Fiorelli, G
Mannucci, P M
Idéo, G
Producer:
19670730
In:
Enzymologia biologica et clinica
vol. 7
Online resources:
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16.
Cholesterol HDL in G-6-PD deficient newborn infants following phenobarbital administration.
[electronic resource]
by
Dessi, S
Porcu, M
Andria, C
Batetta, B
Altieri, M
Pani, P
Macciotta, A
Producer:
19820109
In:
Research communications in chemical pathology and pharmacology
vol. 33
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17.
Effect of phenobarbital treatment on erythrocyte glucose-6-phosphate dehydrogenase in human newborns.
[electronic resource]
by
Laconi, E
Dessì, S
Batetta, B
Pani, P
Pirisi, L
Andria, C
Macciotta, A
Producer:
19840611
In:
Pediatric pharmacology (New York, N.Y.)
vol. 3
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18.
Alpha-thalassemia in premature newborns.
[electronic resource]
by
Maccioni, L
Galanello, R
Ruggeri, R
Puddu, R
Rosatelli, D
Marras, A
Chiappe, S
Macciotta, A
Cao, A
Producer:
19870203
In:
Pediatric research
vol. 20
Online resources:
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19.
Homozygous non-deletion alpha 2 globin gene mutation (initiation codon mutation): clinical and haematological phenotype.
[electronic resource]
by
Galanello, R
Monne, M I
Paderi, L
Paglietti, E
Atzori, G
Addis, M
Limongelli, O
Macciotta, A
Cao, A
Producer:
19911113
In:
British journal of haematology
vol. 79
Online resources:
Available from publisher's website
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