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Results: 1-9 |
Results: 9
Magnetic resonance spectroscopy and magnetic resonance imaging findings inKrabbe's disease
Authors: Zarifi, MK Tzika, AA Astrakas, LG Poussaint, TY Anthony, DC Darras, BT
Citation: Mk. Zarifi et al., Magnetic resonance spectroscopy and magnetic resonance imaging findings inKrabbe's disease, J CHILD NEU, 16(7), 2001, pp. 522-526
Exclusion of growth factor gene mutations as a common cause of Sotos syndrome
Authors: Lin, AE Liu, Q Mannheim, GB Darras, BT
Citation: Ae. Lin et al., Exclusion of growth factor gene mutations as a common cause of Sotos syndrome, AM J MED G, 98(1), 2001, pp. 101-102
Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifussmuscular dystrophy
Authors: Brown, CA Lanning, RW McKinney, KQ Salvino, AR Cherniske, E Crowe, CA Darras, BT Gominak, S Greenberg, CR Grosmann, C Heydemann, P Mendell, JR Pober, BR Sasaki, T Shapiro, F Simpson, DA Suchowersky, O Spence, JE
Citation: Ca. Brown et al., Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifussmuscular dystrophy, AM J MED G, 102(4), 2001, pp. 359-367
Diagnosis of pediatric neuromuscular disorders in the era of DNA analysis
Authors: Darras, BT Jones, HR
Citation: Bt. Darras et Hr. Jones, Diagnosis of pediatric neuromuscular disorders in the era of DNA analysis, PED NEUROL, 23(4), 2000, pp. 289-300
Metabolic myopathies: A clinical approach; Part II
Authors: Darras, BT Friedman, NR
Citation: Bt. Darras et Nr. Friedman, Metabolic myopathies: A clinical approach; Part II, PED NEUROL, 22(3), 2000, pp. 171-181
Metabolic myopathies: A clinical approach; Part I
Authors: Darras, BT Friedman, NR
Citation: Bt. Darras et Nr. Friedman, Metabolic myopathies: A clinical approach; Part I, PED NEUROL, 22(2), 2000, pp. 87-97
Acute care pediatric electromyography
Authors: Jones, HR Darras, BT
Citation: Hr. Jones et Bt. Darras, Acute care pediatric electromyography, MUSCLE NERV, 2000, pp. S53-S62
A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy
Authors: Bonnemann, CG Cox, GF Shapiro, F Wu, JJ Feener, CA Thompson, TG Anthony, DC Eyre, DR Darras, BT Kunkel, LM
Citation: Cg. Bonnemann et al., A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy, P NAS US, 97(3), 2000, pp. 1212-1217
Edward F. Rabe, MD (1918-1998) - In memoriam
Authors: Darras, BT Dodge, PR
Citation: Bt. Darras et Pr. Dodge, Edward F. Rabe, MD (1918-1998) - In memoriam, J CHILD NEU, 14(9), 1999, pp. 620-620
Risultati: 1-9 |