iAH Search interface 2.4 - Results of the search <page 1>

Library collection

Database :	article
Search on :	LEMES, AIDA [Author]
References found :	14 [refine]
Displaying:	1 .. 10 in format [ISO 690]

^{page 1 of 2}

^{go to page}

1 / 14

	select
	to print

González, Verónica et al. Porfiria hepato eritropoyética asociada a diabetes mellitus tipo 1. A propósito de un caso clínico. Arch. Pediatr. Urug., Dic 2021, vol.92, no.2. ISSN 1688-1249

· abstract in spanish | english | portuguese · text in spanish

2 / 14

	select
	to print

Rosas, Melania et al. Encefalopatía subaguda adquirida del lactante por deficiencia de vitamina B12 materna. Arch. Pediatr. Urug., 2020, vol.91, no.6, p.348-358. ISSN 1688-1249

· abstract in spanish | english | portuguese · text in spanish

3 / 14

	select
	to print

Cibils, Lucía et al. Asociación de melanocitosis dérmica con enfermedades lisosomales . Arch. Pediatr. Urug., Dic 2016, vol.87, no.4, p.342-346. ISSN 1688-1249

· abstract in spanish | english · text in spanish

4 / 14

	select
	to print

Larrandaburu, Mariela et al. Síndrome de pterigium múltiple: recurrencia en una familia. Arch. Pediatr. Urug., Dic 2009, vol.80, no.4, p.284-290. ISSN 1688-1249

· abstract in spanish | english · text in spanish

5 / 14

	select
	to print

Tambasco, Ricardo et al. Enfermedad de Krabbe: A propósito de un caso clínico . Arch. Pediatr. Urug., Dic 2012, vol.83, no.3, p.189-194. ISSN 1688-1249

· abstract in spanish | english · text in spanish

6 / 14

	select
	to print

Lemes, Aída et al. Pesquisa neonatal. Arch. Pediatr. Urug., Mar 2012, vol.83, no.1, p.40-44. ISSN 1688-1249

· text in spanish

7 / 14

	select
	to print

Lemes, Aída et al. Un fenotipo clínicamente reconocible: síndrome alfa-talasemia con retraso mental ligado al cromosoma X (ATR-X). Análisis clínico y molecular en dos hermanos. Arch. Pediatr. Urug., Jun 2009, vol.80, no.2, p.123-128. ISSN 1688-1249

· abstract in spanish | english · text in spanish

8 / 14

	select
	to print

Russi, María Eugenia et al. Déficit de succínico semialdehído deshidrogenasa: Primer caso de aciduria 4 OH butírica en Uruguay. Arch. Pediatr. Urug., Dic 2006, vol.77, no.4, p.368-372. ISSN 1688-1249

· abstract in spanish | english · text in spanish

9 / 14

	select
	to print

INCORONATO, ANDREA et al. Deficiencia de ornitina transcarbamilasa: presentación de un caso. Arch. Pediatr. Urug., 2005, vol.76, no.3, p.234-238. ISSN 1688-1249

· abstract in spanish | english · text in spanish

10 / 14

	select
	to print

LEMES, AíDA. Errores congénitos del metabolismo. Arch. Pediatr. Urug., Mar 2003, vol.74, no.1, p.33-36. ISSN 1688-1249

· text in spanish

^{page 1 of 2}

^{go to page}

Refine the search

Database : article

Advanced form

Search for : Free form Basic form

	Search	in field
1
2
3

Search engine: iAH powered by WWWISIS

BIREME/PAHO/WHO - Latin American and Caribbean Center on Health Sciences Information