Biotinidase deficiency in Pakistani children; what needs to be known and done.

[1]  S. Bhate,et al.  Two unusual clinical and radiological presentations of biotinidase deficiency. , 2010, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

[2]  B. Wolf Clinical issues and frequent questions about biotinidase deficiency. , 2010, Molecular genetics and metabolism.

[3]  B. Wolf Worldwide survey of neonatal screening for biotinidase deficiency , 1991, Journal of Inherited Metabolic Disease.

[4]  J. Leonard,et al.  Biotinidase Deficiency: a Treatable Leukoencephalopathy , 2004, Neuropediatrics.

[5]  J. G. Alvarez,et al.  Cutaneous and neurologic manifestations of biotinidase deficiency , 2000, International journal of dermatology.

[6]  T. Suormala,et al.  Delayed-onset profound biotinidase deficiency. , 1998, The Journal of pediatrics.

[7]  B. Wolf,et al.  Screening for biotinidase deficiency in newborns: worldwide experience. , 1990, Pediatrics.

[8]  K. Bartlett,et al.  Biotinidase deficiency: a survey of 10 cases. , 1988, Archives of disease in childhood.

[9]  B. Wolf,et al.  Biotinidase deficiency: Initial clinical features and rapid diagnosis , 1985, Annals of neurology.