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Boletín Médico del Hospital Infantil de México

2010, Number 1

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Bol Med Hosp Infant Mex 2010; 67 (1)

Newborn with spinal muscular atrophy and hypoxic-ischemic encephalopathy

Sánchez MJ, Moreno GAM, Romero BBL, Hernández AJ, García DC, Sánchez AA

Language: Spanish
References: 21
Page: 63-73
PDF size: 438.43 Kb.


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REFERENCES

  1. Vintzileos AM, et al. The relationship between fetal biophysical profile and cord pH in patients undergoing cesarean section before the onset of labor. Obstet and Gyn 1987;70:196-201.

  2. Rufo-Campos, et al. Encefalopatía hipóxico-isquémica del recién nacido a término. Recientes avances, marcadores de hipoxia y opciones terapéuticas. Rev Neurol 2000;31:617-623.

  3. Castro-Gago M, et al. Parámetros bioquímicos predictivos de daño neuronal en la edad pediátrica. Rev Neurol 2001;32:1141-1150.

  4. Graham E, Ruis K, Hartman A, Northington F, Fox H. A systematic review of the role of intrapartum hypoxia-ischemia in the causation of neonatal encephalopathy. Am J Obstet & Gyn 2008;199:587-595.

  5. Brunton L, et al. Goodman & Gilman’s The Pharmacological Basis of Therapeutics. McGraw Hill. 11ª ed. EUA, 2005.pp.1073-1103.

  6. Normas y Procedimientos de Neonatología. Instituto Nacional de Perinatología. INPer, 2003.pp.180-184.

  7. Secretaría de Salud, Asociación Nacional de Medicina Transfusional A.C. Guía para el uso clínico de la sangre. 3a ed. 2007,p.p. 10-20.

  8. Lichtman M, Beutler E, Kaushansky K. Williams Hematology. 7a ed. Edit. McGraw Hill. pp. 375-391.

  9. Igarashi M. Floppy infant syndrome. J Clin Neuromusc Dis 2004;6:69-90.

  10. Erazo-Torricelli R. Hipotonía neonatal. Rev Neurol 2000;31:252-262.

  11. Alfonso I, et al. Hipotonía neonatal generalizada. Rev Neurol 2003;37:228-239.

  12. Prats-Viñas J. Enfoque diagnóstico del niño hipotónico. Protocolos Diagnóstico Terapéuticos de la AEP: Neurología Pediátrica 2008.

  13. Núñez A, et al. Síndrome hipotónico del recién nacido. Rev Chil Pediatr 2008;79:146-151.

  14. Rimoin D, et al. Emery and Rimoin´s Principles and Practice of Medical Genetics. 5° edición. 2007:3001-3023.

  15. Fenichel Geerald M, Hypotonic Infant. In: Clinical Pediatric Neurology, Chapter 6, 5th edition. Elservier Saunders, Philadelphia, Pennsylvania, USA, 2005.

  16. Swaiman K. Muscular tone and Gait Disturbance in. Pediatric neurology: Principles & Practice. Chapter 5, Vol. 1, 4th ed. St. Louis, Missouri: Mosby Elselver, USA, 2006.p. 65-69.

  17. Zerros K, Rudnik-Schöneborn S. Natural history in proximal spinal muscular atrophy (SMT): Clinical analysis of 415 patients and suggestions for a modification of existing classifications. Arch Neurol 1995;52:518-523.

  18. Ogino S, Wilson RB. Genetic testing and risk assessment for spinal muscular atrophy (SMA). Hum Genet 2002;111:477-500.

  19. Ogino S, Wilson RB. Spinal muscular atrophy: molecular genetics and diagnostics. Expert Rev Mol Diagn 2004;4:15-29.

  20. Alías L, et al. Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene. Hum Genet 2009;125:29-39.

  21. Daniels G, et al. Six unaffected livebirths following preimplantation diagnosis for spinal muscular atrophy. Mol Hum Reprod 2001;7:995-1000.




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