메뉴 건너뛰기




Volumn 15, Issue 1, 2008, Pages 10-20

The Evaluation of the Hypotonic Infant

Author keywords

[No Author keywords available]

Indexed keywords

ANTERIOR HORN CELL; ARTICLE; BRAIN MALFORMATION; CLINICAL EVALUATION; CLINICAL FEATURE; DEMYELINATION; DEVELOPMENTAL DISORDER; HUMAN; INFANT; INFANTILE HYPOTONIA; MUSCLE TONE; MUSCULAR DYSTROPHY; NEUROMUSCULAR SYNAPSE; PERIPHERAL NERVE; SYSTEMIC DISEASE;

EID: 40649102940     PISSN: 10719091     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.spen.2008.01.003     Document Type: Article
Times cited : (95)

References (21)
  • 1
    • 0020008014 scopus 로고
    • The newborn with poor muscle tone
    • Fenichel G.M. The newborn with poor muscle tone. Sem Perinatol 6 (1982) 68-88
    • (1982) Sem Perinatol , vol.6 , pp. 68-88
    • Fenichel, G.M.1
  • 3
    • 40649115377 scopus 로고    scopus 로고
    • Symptoms of Neurologic Disorders: Neurologic Symptoms
    • Finberg L., and Kleinman R.E. (Eds), Saunders, Philadelphia, PA
    • Bodensteiner J.B. Symptoms of Neurologic Disorders: Neurologic Symptoms. In: Finberg L., and Kleinman R.E. (Eds). Saunders Manual of Pediatric Practice (2002), Saunders, Philadelphia, PA 953-955
    • (2002) Saunders Manual of Pediatric Practice , pp. 953-955
    • Bodensteiner, J.B.1
  • 4
    • 40649125983 scopus 로고    scopus 로고
    • Neurologic Examination
    • Finberg L., and Kleinman R.E. (Eds), Saunders, Philadelphia, PA
    • Bodensteiner J.B. Neurologic Examination. In: Finberg L., and Kleinman R.E. (Eds). Saunders Manual of Pediatric Practice (2002), Saunders, Philadelphia, PA 1017-1018
    • (2002) Saunders Manual of Pediatric Practice , pp. 1017-1018
    • Bodensteiner, J.B.1
  • 5
    • 40649097697 scopus 로고    scopus 로고
    • Neurologic examination of the neonate
    • Finberg L., and Kleinman R.E. (Eds), Saunders, Philadelphia, PA
    • Bodensteiner J.B. Neurologic examination of the neonate. In: Finberg L., and Kleinman R.E. (Eds). Saunders Manual of Pediatric Practice (2002), Saunders, Philadelphia, PA 1018-1020
    • (2002) Saunders Manual of Pediatric Practice , pp. 1018-1020
    • Bodensteiner, J.B.1
  • 6
    • 40649128711 scopus 로고    scopus 로고
    • Congenital myopathies
    • Katurji B., Kaminski H.J., and Preston D.C. (Eds), Butterworth Heinemann, Newton, MA
    • Bodensteiner J.B., Riggs J.E., and Schochet S.S. Congenital myopathies. In: Katurji B., Kaminski H.J., and Preston D.C. (Eds). Neuromuscular Diseases (2002), Butterworth Heinemann, Newton, MA 1114-1127
    • (2002) Neuromuscular Diseases , pp. 1114-1127
    • Bodensteiner, J.B.1    Riggs, J.E.2    Schochet, S.S.3
  • 7
  • 8
    • 0030930431 scopus 로고    scopus 로고
    • The macrocerebellum: Neuroimaging and clinical features of a newly recognized condition
    • Bodensteiner J.B., Schaefer G.B., Keller G.M., et al. The macrocerebellum: Neuroimaging and clinical features of a newly recognized condition. J Child Neurol 12 (1997) 365-368
    • (1997) J Child Neurol , vol.12 , pp. 365-368
    • Bodensteiner, J.B.1    Schaefer, G.B.2    Keller, G.M.3
  • 10
    • 0016260316 scopus 로고
    • Hypoactive labyrinths and motor development
    • Rapin I. Hypoactive labyrinths and motor development. Clin Pediatr 13 (1974) 922-937
    • (1974) Clin Pediatr , vol.13 , pp. 922-937
    • Rapin, I.1
  • 11
    • 0038407686 scopus 로고    scopus 로고
    • Hypotonia, congenital hearing loss and hypoactive labyrinths
    • Bodensteiner J.B., Smith D.S., and Schaefer G.B. Hypotonia, congenital hearing loss and hypoactive labyrinths. J Child Neurol 18 (2003) 171-174
    • (2003) J Child Neurol , vol.18 , pp. 171-174
    • Bodensteiner, J.B.1    Smith, D.S.2    Schaefer, G.B.3
  • 12
    • 33847214592 scopus 로고    scopus 로고
    • Role of cytogenetics and molecular cytogenetics in the diagnosis of genetic imbalances
    • Bhavana J.D., and Sanger W.G. Role of cytogenetics and molecular cytogenetics in the diagnosis of genetic imbalances. Semin Pediatr Neurol 14 (2007) 2-6
    • (2007) Semin Pediatr Neurol , vol.14 , pp. 2-6
    • Bhavana, J.D.1    Sanger, W.G.2
  • 13
    • 0020554379 scopus 로고
    • Evolution of nerve conduction abnormalities in children with autosomal dominant hypertrophic neuropathy of the Charcot-Marie-Tooth type
    • Gutmann L., Fakadej A., and Riggs J.E. Evolution of nerve conduction abnormalities in children with autosomal dominant hypertrophic neuropathy of the Charcot-Marie-Tooth type. Muscle Nerve 6 (1983) 515-519
    • (1983) Muscle Nerve , vol.6 , pp. 515-519
    • Gutmann, L.1    Fakadej, A.2    Riggs, J.E.3
  • 14
    • 0014996232 scopus 로고
    • Malattia di Charcot-Marie-Tooth ad insorgenza precoce presentazione di una famiglia
    • Zellweger H., Schochet S., Pavone L., et al. Malattia di Charcot-Marie-Tooth ad insorgenza precoce presentazione di una famiglia. Pediatria 79 (1971) 198-214
    • (1971) Pediatria , vol.79 , pp. 198-214
    • Zellweger, H.1    Schochet, S.2    Pavone, L.3
  • 15
    • 18744401389 scopus 로고    scopus 로고
    • Current understanding of congenital myasthenic syndromes
    • Engel A.G., and Sine S.M. Current understanding of congenital myasthenic syndromes. Curr Opin Pharmacol 5 (2005) 308-321
    • (2005) Curr Opin Pharmacol , vol.5 , pp. 308-321
    • Engel, A.G.1    Sine, S.M.2
  • 16
    • 21244453035 scopus 로고    scopus 로고
    • 126th International Workshop: Congenital myasthenic syndromes, 24-26 September 2004, Naarden, the Netherlands
    • Beeson D., Hantai D., Lochmuller H., et al. 126th International Workshop: Congenital myasthenic syndromes, 24-26 September 2004, Naarden, the Netherlands. Neuromuscul Disord 15 (2005) 498-512
    • (2005) Neuromuscul Disord , vol.15 , pp. 498-512
    • Beeson, D.1    Hantai, D.2    Lochmuller, H.3
  • 17
    • 0032560851 scopus 로고    scopus 로고
    • An ancient retrotransposalinsertion causes Fukuyama-type congenital muscular dystrophy
    • Kobayashi K., Nakahori Y., Miyake M., et al. An ancient retrotransposalinsertion causes Fukuyama-type congenital muscular dystrophy. Nature 394 (1998) 388-392
    • (1998) Nature , vol.394 , pp. 388-392
    • Kobayashi, K.1    Nakahori, Y.2    Miyake, M.3
  • 18
    • 1042268038 scopus 로고    scopus 로고
    • The congenital and limb-girdle muscular dystrophies: Sharpening the focus, blurring the boundaries
    • Kirschner J., and Bonnemann C.G. The congenital and limb-girdle muscular dystrophies: Sharpening the focus, blurring the boundaries. Arch Neurol 61 (2004) 189-199
    • (2004) Arch Neurol , vol.61 , pp. 189-199
    • Kirschner, J.1    Bonnemann, C.G.2
  • 19
    • 0033794412 scopus 로고    scopus 로고
    • Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: Evidence for a novel CMD syndrome
    • Villanova M., Mercuri E., Bertini E., et al. Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: Evidence for a novel CMD syndrome. Neuromuscul Disord 10 (2000) 541-547
    • (2000) Neuromuscul Disord , vol.10 , pp. 541-547
    • Villanova, M.1    Mercuri, E.2    Bertini, E.3
  • 20
    • 0031594947 scopus 로고    scopus 로고
    • Laminin alpha2 muscular dystrophy: Genotype/phenotype studies of 22 patients
    • Pegoraro E., Marks H., Garcia C.A., et al. Laminin alpha2 muscular dystrophy: Genotype/phenotype studies of 22 patients. Neurology 51 (1998) 101-110
    • (1998) Neurology , vol.51 , pp. 101-110
    • Pegoraro, E.1    Marks, H.2    Garcia, C.A.3
  • 21
    • 4444234437 scopus 로고    scopus 로고
    • The congenital muscular dystrophies in 2004: A century of exciting progress
    • Muntoni F., and Voit T. The congenital muscular dystrophies in 2004: A century of exciting progress. Neuromuscul Disord 14 (2004) 635-649
    • (2004) Neuromuscul Disord , vol.14 , pp. 635-649
    • Muntoni, F.1    Voit, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.