19p13.3 Aberrations Are Associated with Dysmorphic Features and Deviant Psychomotor Development.
- Published in:
- Cytogenetic & Genome Research, 2010, v. 132, n. 1/2, p. 8, doi. 10.1159/000320920
- By:
- Publication type:
- Article
Works matching AU Näntö-Salonen K
Results: 15
1
2
Early seroconversion and rapidly increasing autoantibody concentrations predict prepubertal manifestation of type 1 diabetes in children at genetic risk.
- Published in:
- Diabetologia, 2012, v. 55, n. 7, p. 1926, doi. 10.1007/s00125-012-2523-3
- By:
- Publication type:
- Article
3
Characterization of the perivascular reticulin network in a case of primary brain lymphoma.
- Published in:
- Acta Neuropathologica, 1985, v. 66, n. 4, p. 299, doi. 10.1007/BF00690962
- By:
- Publication type:
- Article
4
Neurofibromatosis tumor and skin cells in culture.
- Published in:
- Acta Neuropathologica, 1984, v. 63, n. 4, p. 269, doi. 10.1007/BF00687332
- By:
- Publication type:
- Article
5
Nutrient intake in lysinuric protein intolerance.
- Published in:
- Journal of Inherited Metabolic Disease, 2007, v. 30, n. 5, p. 716, doi. 10.1007/s10545-007-0558-2
- By:
- Publication type:
- Article
6
Oral lysine feeding in gyrate atrophy with hyperornithinaemia – A pilot study.
- Published in:
- Journal of Inherited Metabolic Disease, 2000, v. 23, n. 4, p. 305, doi. 10.1023/A:1005638004530
- By:
- Publication type:
- Article
7
Central nervous system involvement in gyrate atrophy of the choroid and retina with hyperornithinaemia.
- Published in:
- Journal of Inherited Metabolic Disease, 1999, v. 22, n. 8, p. 855, doi. 10.1023/A:1005602405349
- By:
- Publication type:
- Article
8
Varicella and varicella immunity in patients with lysinuric protein intolerance.
- Published in:
- Journal of Inherited Metabolic Disease, 1998, v. 21, n. 2, p. 103, doi. 10.1023/A:1005335423939
- By:
- Publication type:
- Article
9
Partial epilepsy in a girl with a symptom-free sister: First two Finnish patients with dihydropyrimidine dehydrogenase deficiency.
- Published in:
- Journal of Inherited Metabolic Disease, 1997, v. 20, n. 5, p. 719, doi. 10.1023/A:1005399131620
- By:
- Publication type:
- Article
10
Abnormal Dermal Proteoglycan in Aspartylglycosaminuria: A Possible Mechanism for Ultrastructural Changes of Collagen Fibrils in a Glycoprotein Storage Disorder.
- Published in:
- Connective Tissue Research, 1987, v. 16, n. 4, p. 367, doi. 10.3109/03008208709005621
- By:
- Publication type:
- Article
11
Development of overweight in an atherosclerosis prevention trial starting in early childhood. The STRIP study.
- Published in:
- International Journal of Obesity, 2006, v. 30, n. 4, p. 618, doi. 10.1038/sj.ijo.0803249
- By:
- Publication type:
- Article
12
Serum type III procollagen in children with type I hereditary tyrosinemia.
- Published in:
- 1999
- By:
- Publication type:
- journal article
13
Suppression of GH secretion in pituitary gigantism by continuous subcutaneous octreotide infusion in a pubertal boy.
- Published in:
- Acta Paediatrica, 1999, v. 88, n. 1, p. 29, doi. 10.1111/j.1651-2227.1999.tb01263.x
- By:
- Publication type:
- Article
14
Noninvasive diagnosis of focal hyperinsulinism of infancy with [18F]-DOPA positron emission tomography.
- Published in:
- 2006
- By:
- Publication type:
- Journal Article
15
Abnormal coagulation and enhanced fibrinolysis due to lysinuric protein intolerance associates with bleeds and renal impairment.
- Published in:
- Haemophilia, 2018, v. 24, n. 5, p. e312, doi. 10.1111/hae.13543
- By:
- Publication type:
- Article