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Transactions of the American Neurological Association
|
January 1, 1974
Heterogeneity in two families with central core disease
E M Brett, J A Morgan-Hughes, B D Lake
Experimental Neurology
|
March 1, 1983
Possible manifestation of the dystrophic X chromosome in muscle cultures from carriers of Duchenne muscular dystrophy
E J Thompson, R Yasin, B D Lake, et al.
American Journal of Medical Genetics
|
June 5, 1995
Late-infantile Batten disease: purification of the subunit c of the mitochondrial ATP synthase from storage material
K Hagopian, B D Lake, B G Winchester, et al.
Prenatal Diagnosis
|
September 1, 1993
Fetal tissue involvement in the late infantile type of neuronal ceroid lipofuscinosis
C W Chow, J Borg, V R Billson, et al.
Brain : a Journal of Neurology
|
January 1, 1973
A neurovisceral storage disease with vertical supranuclear ophthalmoplegia, and its relationship to Niemann-Pick disease. A report of nine patients
B G Neville, B D Lake, R Stephens, et al.
Journal of Medical Genetics
|
June 1, 1986
Tel Hashomer camptodactyly syndrome: report of a case with myopathic features
M A Patton, K D McDermot, B D Lake, et al.
Acta Neuropathologica
|
December 21, 1976
Cerebral malformation associated with metabolic disorder. A report of 2 cases
M Erdohazi, N D Barnes, M J Robinson, et al.
Archives of Pathology & Laboratory Medicine
|
May 1, 1978
Hirschsprung's disease: an appraisal of histochemically demonstrated acetylcholinesterase activity in suction rectal biopsy specimens as an aid to diagnosis
B D Lake, P Puri, H H Nixon, et al.
Archives of Disease in Childhood
|
March 1, 1982
Metachromatic leucodystrophy: review of 38 cases
R MacFaul, N Cavanagh, B D Lake, et al.
Histopathology
|
December 1, 1992
Intestinal pseudo-obstruction with deficient smooth muscle alpha-actin
V V Smith, B D Lake, M A Kamm, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 136) with videos related to
Sort By:
Page
of 14
Transactions of the American Neurological Association
|
January 1, 1974
Heterogeneity in two families with central core disease
E M Brett, J A Morgan-Hughes, B D Lake
Experimental Neurology
|
March 1, 1983
Possible manifestation of the dystrophic X chromosome in muscle cultures from carriers of Duchenne muscular dystrophy
E J Thompson, R Yasin, B D Lake, et al.
American Journal of Medical Genetics
|
June 5, 1995
Late-infantile Batten disease: purification of the subunit c of the mitochondrial ATP synthase from storage material
K Hagopian, B D Lake, B G Winchester, et al.
Prenatal Diagnosis
|
September 1, 1993
Fetal tissue involvement in the late infantile type of neuronal ceroid lipofuscinosis
C W Chow, J Borg, V R Billson, et al.
Brain : a Journal of Neurology
|
January 1, 1973
A neurovisceral storage disease with vertical supranuclear ophthalmoplegia, and its relationship to Niemann-Pick disease. A report of nine patients
B G Neville, B D Lake, R Stephens, et al.
Journal of Medical Genetics
|
June 1, 1986
Tel Hashomer camptodactyly syndrome: report of a case with myopathic features
M A Patton, K D McDermot, B D Lake, et al.
Acta Neuropathologica
|
December 21, 1976
Cerebral malformation associated with metabolic disorder. A report of 2 cases
M Erdohazi, N D Barnes, M J Robinson, et al.
Archives of Pathology & Laboratory Medicine
|
May 1, 1978
Hirschsprung's disease: an appraisal of histochemically demonstrated acetylcholinesterase activity in suction rectal biopsy specimens as an aid to diagnosis
B D Lake, P Puri, H H Nixon, et al.
Archives of Disease in Childhood
|
March 1, 1982
Metachromatic leucodystrophy: review of 38 cases
R MacFaul, N Cavanagh, B D Lake, et al.
Histopathology
|
December 1, 1992
Intestinal pseudo-obstruction with deficient smooth muscle alpha-actin
V V Smith, B D Lake, M A Kamm, et al.
Page
of 14