Similar articles for PMID: 20432825

Year	Number of Results
1954	1
1964	1
1965	1
1969	5
1970	4
1971	1
1972	3
1973	3
1974	3
1976	2
1978	1
1979	1
1980	3
1981	1
1982	3
1983	2
1984	3
1986	3
1987	2
1988	4
1989	1
1991	2
1992	5
1993	1
1994	1
1995	3
1997	2
1999	3
2000	1
2002	1
2003	2
2004	1
2006	1
2007	2
2008	1
2009	4
2010	5
2011	2
2012	2
2013	1
2014	5
2015	1
2016	3
2017	4
2018	5
2019	3
2020	1
2022	1
2023	1
2024	0

1

Esophageal atresia concomitant with congenital hypothyroidism and phenylketonuria in a newborn.

Peker E, Tuncer O, Cagan E, Dogan M, Kaya A, Avcu S, Kirimi E. Peker E, et al. J Pediatr Endocrinol Metab. 2010 Jan-Feb;23(1-2):203-4. doi: 10.1515/jpem.2010.23.1-2.203. J Pediatr Endocrinol Metab. 2010. PMID: 20432825 No abstract available.

2

Oesophageal atresia in a cretin.

Lister J. Lister J. Proc R Soc Med. 1969 Nov;62(11 Part 1):1094-5. Proc R Soc Med. 1969. PMID: 5356858 Free PMC article. No abstract available.

3

[Pilot experiment concerning the concomitant detection of congenital hypothyroidism and phenylketonuria in newborn infants in a high-risk geographical zone. (Results for the year 1979)].

Prişcu AR, Manolescu E, Sichitiu S, Iordăchescu F, Tomescu E, Stamate M, Ciurea A, Poboran V, Iacob C, Bugariu E, Milcu M, Caniola I, Gasparovici L, Bucur I, Stefanache O, Georgescu BG, Zaharescu J, Opriş CC, Pältineau V, Horincaru N, Wirtz A, Terţan I, Szabo I, Tamas N. Prişcu AR, et al. Rev Pediatr Obstet Ginecol Pediatr. 1980 Apr-Jun;29(2):131-8. Rev Pediatr Obstet Ginecol Pediatr. 1980. PMID: 6776606 Romanian. No abstract available.

4

TAR syndrome and esophagial atresia: a concomitant or variant condition?

Peker E, Cagan E, Dogan M, Sal E, Kirimi E. Peker E, et al. J Matern Fetal Neonatal Med. 2011 Feb;24(2):226-8. doi: 10.3109/14767058.2010.482603. Epub 2010 May 17. J Matern Fetal Neonatal Med. 2011. PMID: 20476878

5

[Clinical aspects of phenylketonuria].

Blehová B, Pazoutová N, Rákosníková M, Jirásek J. Blehová B, et al. Cas Lek Cesk. 1972;111(8):170-2. Cas Lek Cesk. 1972. PMID: 4258699 Czech. No abstract available.

6

Family studies on congenital esophageal atresia with or without tracheoesophageal fistula.

Chen H, Goei GS, Hertzler JH. Chen H, et al. Birth Defects Orig Artic Ser. 1979;15(5C):117-44. Birth Defects Orig Artic Ser. 1979. PMID: 393323 Review. No abstract available.

7

Esophageal atresia with tracheoesophageal fistula in mother and child.

Engel PM, Vos LJ, de Vries JA, Kuijjer PJ. Engel PM, et al. J Pediatr Surg. 1970 Oct;5(5):564-5. doi: 10.1016/0022-3468(70)90011-4. J Pediatr Surg. 1970. PMID: 5505694 No abstract available.

8

[A case of esophageal atresia with multiple abnormalities in a newborn twin].

Moro G, Gesmundo R, Bevilacqua A, Maiullari E, Gandini R. Moro G, et al. Minerva Chir. 1988 Jun 15;43(11):993-5. Minerva Chir. 1988. PMID: 3173714 Italian. No abstract available.

9

Phenylketonuria and neonatal hypothyroidism in Spain. Priority of screening for neonatal hypothyroidism.

Frontera-Izquierdo P. Frontera-Izquierdo P. Eur J Pediatr. 1980 May;133(3):297. doi: 10.1007/BF00496094. Eur J Pediatr. 1980. PMID: 7389745 No abstract available.

10

[Examination of newborn infants in the first week. Techniques and objectives including early and systematic screening of congenital hypothyroidism and phenylketonuria].

Lequien P. Lequien P. Rev Prat. 1991 Feb 1;41(4):357-60. Rev Prat. 1991. PMID: 2008589 French. No abstract available.

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