Hagenfeldt L - Search Results

1

[Acute metabolic critical conditions in hereditary metabolic diseases].

von Döbeln U, Larsson A, Hagenfeldt L. von Döbeln U, et al. Among authors: hagenfeldt l. Lakartidningen. 1989 Aug 30;86(35):2849-50. Lakartidningen. 1989. PMID: 2796465 Swedish. No abstract available.

2

[B12 deficiency in breast-fed children. Maternal deficiency may cause severe symptoms in children].

Navér L, von Döbeln U, Hagenfeldt L. Navér L, et al. Among authors: hagenfeldt l. Lakartidningen. 1995 Sep 13;92(37):3331-4. Lakartidningen. 1995. PMID: 7674731 Swedish. No abstract available.

3

Pyroglutamic aciduria. Studies in an infant with chronic metabolic acidosis.

Hagenfeldt L, Larsson A, Zetterström R. Hagenfeldt L, et al. Acta Paediatr Scand. 1974 Jan;63(1):1-8. doi: 10.1111/j.1651-2227.1974.tb04342.x. Acta Paediatr Scand. 1974. PMID: 4830407 No abstract available.

4

[Screening for congenital hypothyreosis. Report of a nationwide experimental study].

Larsson A, Hagenfeldt L, Westphal O, Alm J, Mortensson W. Larsson A, et al. Among authors: hagenfeldt l. Lakartidningen. 1982 Jan 27;79(4):221-4. Lakartidningen. 1982. PMID: 7087616 Swedish. No abstract available.

5

Retrospective diagnosis of 3-hydroxydicarboxylic aciduria by analysis of filter paper blood samples.

von Döbeln U, Venizelos N, Hagenfeldt L. von Döbeln U, et al. Among authors: hagenfeldt l. J Inherit Metab Dis. 1990;13(2):165-8. doi: 10.1007/BF01799680. J Inherit Metab Dis. 1990. PMID: 2143242

6

3-Hydroxydicarboxylic aciduria--a fatty acid oxidation defect with severe prognosis.

Hagenfeldt L, von Döbeln U, Holme E, Alm J, Brandberg G, Enocksson E, Lindeberg L. Hagenfeldt L, et al. J Pediatr. 1990 Mar;116(3):387-92. doi: 10.1016/s0022-3476(05)82826-4. J Pediatr. 1990. PMID: 2308028

7

[Information from the PKU-section - report of activities 1981].

Hagenfeldt L, Lundberg K, Larsson A, Thuresson M. Hagenfeldt L, et al. Jordemodern. 1982 Sep;95(9):287-90. Jordemodern. 1982. PMID: 6922863 Swedish. No abstract available.

8

Clinical and biochemical presentation of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Hagenfeldt L, Venizelos N, von Döbeln U. Hagenfeldt L, et al. J Inherit Metab Dis. 1995;18(2):245-8. doi: 10.1007/BF00711779. J Inherit Metab Dis. 1995. PMID: 7564259 No abstract available.

9

[The routine sampling procedure for PKU should be changed. Venous puncture is less painful than heel lancing].

Larsson BA, Nörstmo A, Guthenberg C, Olsson GL, Danielsson P, Hagenfeldt L, Elander G, Larsson A. Larsson BA, et al. Among authors: hagenfeldt l. Lakartidningen. 1997 Dec 3;94(49):4625-8. Lakartidningen. 1997. PMID: 9445935 Review. Swedish.

10

Two missense mutations causing mild hyperphenylalaninemia associated with DNA haplotype 12.

Svensson E, Eisensmith RC, Dworniczak B, von Döbeln U, Hagenfeldt L, Horst J, Woo SL. Svensson E, et al. Among authors: hagenfeldt l. Hum Mutat. 1992;1(2):129-37. doi: 10.1002/humu.1380010208. Hum Mutat. 1992. PMID: 1301200

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