Found: 17
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Comorbidity in severe developmental language disorders: neuropediatric and psychological considerations.
- Published in:
- 2005
- By:
- Publication type:
- journal article
Mutations and sequence variation in the human myosin heavy chain IIa gene (MYH2).
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 5, p. 617, doi. 10.1038/sj.ejhg.5201375
- By:
- Publication type:
- Article
BOOK REVIEW.
- Published in:
- Acta Paediatrica, 1989, v. 78, n. 4, p. 656, doi. 10.1111/j.1651-2227.1989.tb17960.x
- By:
- Publication type:
- Article
Diagnosis and management of glutaric aciduria type I - revised recommendations.
- Published in:
- Journal of Inherited Metabolic Disease, 2011, v. 34, n. 3, p. 677, doi. 10.1007/s10545-011-9289-5
- By:
- Publication type:
- Article
Bengt Hagberg (1923-2015), Swedish father of child neurology.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Bengt Hagberg.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Old and New Entities with Rett or Angelman-Like Intellectual Disability.
- Published in:
- 2012
- By:
- Publication type:
- Book Review
Aetiology of severe mental retardation and further genetic analysis by high-resolution microarray in a population-based series of 6- to 17-year-old children.
- Published in:
- Acta Paediatrica, 2012, v. 101, n. 1, p. 85, doi. 10.1111/j.1651-2227.2011.02417.x
- By:
- Publication type:
- Article
Beckung and Kyllerman reply.
- Published in:
- Developmental Medicine & Child Neurology, 2005, v. 47, n. 2, p. 143, doi. 10.1017/S001216220522025X
- By:
- Publication type:
- Article
Motor impairments, neurological signs, and developmental level in individuals with Angelman syndrome.
- Published in:
- 2004
- By:
- Publication type:
- journal article
Motor impairments, neurological signs, and developmental level in individuals with Angelman syndrome.
- Published in:
- Developmental Medicine & Child Neurology, 2004, v. 46, n. 4, p. 239, doi. 10.1017/S0012162204000398
- By:
- Publication type:
- Article
Induced shift in myosin heavy chain expression in myosin myopathy by endurance training.
- Published in:
- Journal of Neurology, 2004, v. 251, n. 2, p. 179, doi. 10.1007/s00415-004-0295-5
- By:
- Publication type:
- Article
Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy.
- Published in:
- Acta Neuropathologica, 2000, v. 100, n. 1, p. 23, doi. 10.1007/s004010051188
- By:
- Publication type:
- Article
Familial mental retardation and progressive spasticity.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 107, doi. 10.1111/j.1399-0004.1995.tb03936.x
- By:
- Publication type:
- Article
X-linked myotubular myopathy: a linkage study.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 5, p. 335, doi. 10.1111/j.1399-0004.1990.tb03515.x
- By:
- Publication type:
- Article
Diagnosis of Epstein-Barr virus-induced central nervous system infections by DNA amplification from cerebrospinal fluid.
- Published in:
- Annals of Neurology, 1994, v. 35, n. 5, p. 631, doi. 10.1002/ana.410350522
- By:
- Publication type:
- Article
In Memoriam.
- Published in:
- 2017
- By:
- Publication type:
- Obituary