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B D Lake

Showing results (91-100 of 136) with videos related to

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The British Journal of Dermatology|December 1, 1992
Restrictive dermopathy: a disorder of fibroblastsD G Paige, B D Lake, A J Bailey, et al.
Archives of Disease in Childhood|April 1, 1994
Laryngo-onycho-cutaneous syndrome: an inherited epithelial defectR J Phillips, D J Atherton, M L Gibbs, et al.
The Quarterly Journal of Medicine|January 1, 1971
Hepatic glycogen storage disease. Clinical and laboratory findings in 23 casesJ Spencer-Peet, M E Norman, B D Lake, et al.
Developmental Medicine and Child Neurology|February 1, 1983
Involvement of the central nervous system in congenital muscular dystrophiesJ Egger, B E Kendall, M Erdohazi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1988
The diverse neurological features of Niemann-Pick disease type C: a report of two casesR J Coleman, S A Robb, B D Lake, et al.
Advances in Experimental Medicine and Biology|January 1, 1989
Glycoconjugates in storage cytosomes from ceroid-lipofuscinosis (Batten's disease) and in lipofuscin from old-age brainN A Hall, B D Lake, D N Palmer, et al.
Journal of Inherited Metabolic Disease|January 1, 1978
Disordered intestinal function in glycogen storage diseaseP J Milla, D A Atherton, J V Leonard, et al.
Histopathology|November 1, 1981
Abnormalities of the colonic regulatory peptides in Hirschsprung's diseaseA E Bishop, J M Polak, B D Lake, et al.
Journal of Pediatric Gastroenterology and Nutrition|September 1, 1988
Symptomatic selenium deficiency in a child on home parenteral nutritionD A Kelly, A W Coe, A Shenkin, et al.
The British Journal of Dermatology|October 10, 1998
E210K mutation in the gene encoding the beta3 chain of laminin-5 (LAMB3) is predictive of a phenotype of generalized atrophic benign epidermolysis bullosaJ E Mellerio, R A Eady, D J Atherton, et al.
Pageof 14

Showing results (91-100 of 136) with videos related to

Sort By:
Pageof 14
The British Journal of Dermatology|December 1, 1992
Restrictive dermopathy: a disorder of fibroblastsD G Paige, B D Lake, A J Bailey, et al.
Archives of Disease in Childhood|April 1, 1994
Laryngo-onycho-cutaneous syndrome: an inherited epithelial defectR J Phillips, D J Atherton, M L Gibbs, et al.
The Quarterly Journal of Medicine|January 1, 1971
Hepatic glycogen storage disease. Clinical and laboratory findings in 23 casesJ Spencer-Peet, M E Norman, B D Lake, et al.
Developmental Medicine and Child Neurology|February 1, 1983
Involvement of the central nervous system in congenital muscular dystrophiesJ Egger, B E Kendall, M Erdohazi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1988
The diverse neurological features of Niemann-Pick disease type C: a report of two casesR J Coleman, S A Robb, B D Lake, et al.
Advances in Experimental Medicine and Biology|January 1, 1989
Glycoconjugates in storage cytosomes from ceroid-lipofuscinosis (Batten's disease) and in lipofuscin from old-age brainN A Hall, B D Lake, D N Palmer, et al.
Journal of Inherited Metabolic Disease|January 1, 1978
Disordered intestinal function in glycogen storage diseaseP J Milla, D A Atherton, J V Leonard, et al.
Histopathology|November 1, 1981
Abnormalities of the colonic regulatory peptides in Hirschsprung's diseaseA E Bishop, J M Polak, B D Lake, et al.
Journal of Pediatric Gastroenterology and Nutrition|September 1, 1988
Symptomatic selenium deficiency in a child on home parenteral nutritionD A Kelly, A W Coe, A Shenkin, et al.
The British Journal of Dermatology|October 10, 1998
E210K mutation in the gene encoding the beta3 chain of laminin-5 (LAMB3) is predictive of a phenotype of generalized atrophic benign epidermolysis bullosaJ E Mellerio, R A Eady, D J Atherton, et al.
Pageof 14