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Results of search for 'au:"Batlle, A M"', page 8 of 8
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Authors
Afonso, S G
Araujo, L S
Batlle, A M
Buzaleh, A M
Casas, A
Chinarro, S
De Siervi, A
Enriquez de Salamanca, R
Fukuda, H
Juknat, A A
Kotler, M L
Navone, N M
Paredes, S R
Parera, V E
Polo, C F
Rossetti, M V
Stella, A M
Vazquez, E S
Wider de Xifra, E A
del C Batlle, A M
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Topics
5-Aminolevulinate Synthetase
Aminolevulinic Acid
Ammonia-Lyases
Animals
Female
Heme
Humans
Hydroxymethylbilane Synthase
Kinetics
Liver
Male
Mice
Porphobilinogen Synthase
Porphyrins
antagonists & inhibitors
biosynthesis
drug effects
enzymology
metabolism
pharmacology
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English
g d
Spanish
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141.
Familial porphyria cutanea tarda: characterization of seven novel uroporphyrinogen decarboxylase mutations and frequency of common hemochromatosis alleles.
[electronic resource]
by
Mendez, M
Sorkin, L
Rossetti, M V
Astrin, K H
del C Batlle, A M
Parera, V E
Aizencang, G
Desnick, R J
Producer:
19981223
In:
American journal of human genetics
vol. 63
Online resources:
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142.
Functional associations of genetic variants involved in the clinical manifestation of erythropoietic protoporphyria in the Argentinean population.
[electronic resource]
by
Colombo, F P
Rossetti, M V
Méndez, M
Martínez, J E
Enríquez de Salamanca, R
del C Batlle, A M
Parera, V E
Producer:
20131028
In:
Journal of the European Academy of Dermatology and Venereology : JEADV
vol. 27
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143.
A novel 3D evaluation method for assessing bone to bone relationships in clubfoot.
[electronic resource]
by
Ganesan, B
Yip, J
Al-Jumaily, A
Fong, S S M
Kothe Balasankar, S
Ey Batlle, A M
Fong, K N K
Luximon, A
Producer:
20200810
In:
European review for medical and pharmacological sciences
vol. 23
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144.
Further evidence for an essential histidyl residue at the active site of pig liver 5-aminolevulinic acid dehydratase.
[electronic resource]
by
Fukuda, H
Sopena de Kracoff, Y E
Iñigo, L E
Paredes, S R
Ferramola de Sancovich, A M
Sancovich, H A
Batlle, A M
Producer:
19900507
In:
Journal of enzyme inhibition
vol. 3
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145.
Identification and characterization of hydroxymethylbilane synthase mutations causing acute intermittent porphyria: evidence for an ancestral founder of the common G111R mutation.
[electronic resource]
by
De Siervi, A
Rossetti, M V
Parera, V E
Astrin, K H
Aizencang, G I
Glass, I A
Batlle, A M
Desnick, R J
Producer:
19991105
In:
American journal of medical genetics
vol. 86
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