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- W1490605215 abstract "Guidelines on Diagnosis and Treatment of Alpha-1 Antitrypsin Deficiency The alpha-1 antitrypsin (AAT) deficiency is a rare hereditary condition which is rarely diagnosed in the world, including Argentina. Underdiagnosis is mainly due to lack of Correspondencia: Guillermo Menga Domicilio postal: Finochietto 849 (CP 1272)CABAArg Tel.: 4307-6738 E-mail: mengagaamr@gmail.com Recibido: 12.01.2014 Aceptado: 14.02.2014 RAMR 2014;1:28-46" @default.
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- W1490605215 date "2014-01-03" @default.
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- W1490605215 title "Normativas de diagnóstico y tratamiento del déficit de alfa-1 antitripsina" @default.
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