Larsson A - Search Results

1

Genetic and linkage analysis of familial congenital hypothyroidism: exclusion of linkage to the TSH receptor gene.

Ahlbom BD, Yaqoob M, Larsson A, Ilicki A, Annerén G, Wadelius C. Ahlbom BD, et al. Among authors: larsson a. Hum Genet. 1997 Feb;99(2):186-90. doi: 10.1007/s004390050335. Hum Genet. 1997. PMID: 9048917

2

Circulating thyroid antibodies in congenital hypothyroidism.

Ilicki A, Larsson A, Karlsson FA. Ilicki A, et al. Among authors: larsson a. Acta Paediatr Scand. 1991 Aug-Sep;80(8-9):805-11. doi: 10.1111/j.1651-2227.1991.tb11953.x. Acta Paediatr Scand. 1991. PMID: 1659767

3

Psychological development at 7 years of age in children with congenital hypothyroidism. Timing and dosage of initial treatment.

Ilicki A, Larsson A. Ilicki A, et al. Among authors: larsson a. Acta Paediatr Scand. 1991 Feb;80(2):199-204. doi: 10.1111/j.1651-2227.1991.tb11834.x. Acta Paediatr Scand. 1991. PMID: 2035311

4

[Screening for congenital hypothroidism results in early treatment and good psychomotor development].

Ilicki A, Larsson A. Ilicki A, et al. Among authors: larsson a. Lakartidningen. 1991 May 29;88(22):2062-4. Lakartidningen. 1991. PMID: 2051875 Swedish. No abstract available.

5

The value of neonatal serum thyroglobulin determinations in the follow-up of patients with congenital hypothyroidism.

Ilicki A, Ericsson UB, Larsson A, Mortensson W, Thorell J. Ilicki A, et al. Among authors: larsson a. Acta Paediatr Scand. 1990 Aug-Sep;79(8-9):769-75. doi: 10.1111/j.1651-2227.1990.tb11553.x. Acta Paediatr Scand. 1990. PMID: 2239271

6

Neonatal skeletal maturation in congenital hypothyroidism and its prognostic value for psychomotor development at 3 years in patients treated early.

Ilicki A, Larsson A, Mortensson W. Ilicki A, et al. Among authors: larsson a. Horm Res. 1990;33(6):260-4. doi: 10.1159/000181532. Horm Res. 1990. PMID: 2289785

7

Psychomotor development of children with congenital hypothyroidism diagnosed by neonatal screening.

Ilicki A, Larsson A. Ilicki A, et al. Among authors: larsson a. Acta Paediatr Scand. 1988 Jan;77(1):142-7. doi: 10.1111/j.1651-2227.1988.tb10613.x. Acta Paediatr Scand. 1988. PMID: 2453105

8

Galactosemia caused by a point mutation that activates cryptic donor splice site in the galactose-1-phosphate uridyltransferase gene.

Wadelius C, Lagerkvist A, Molin AK, Larsson A, von Döbeln U, Pettersson U. Wadelius C, et al. Among authors: larsson a. Genomics. 1993 Aug;17(2):525-6. doi: 10.1006/geno.1993.1363. Genomics. 1993. PMID: 8406510 No abstract available.

9

Linear growth in early treated children with congenital hypothyroidism.

Heyerdahl S, Ilicki A, Karlberg J, Kase BF, Larsson A. Heyerdahl S, et al. Among authors: larsson a. Acta Paediatr. 1997 May;86(5):479-83. doi: 10.1111/j.1651-2227.1997.tb08917.x. Acta Paediatr. 1997. PMID: 9183486

10

Missense mutations in the human glutathione synthetase gene result in severe metabolic acidosis, 5-oxoprolinuria, hemolytic anemia and neurological dysfunction.

Dahl N, Pigg M, Ristoff E, Gali R, Carlsson B, Mannervik B, Larsson A, Board P. Dahl N, et al. Among authors: larsson a. Hum Mol Genet. 1997 Jul;6(7):1147-52. doi: 10.1093/hmg/6.7.1147. Hum Mol Genet. 1997. PMID: 9215686

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