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T P Mann

Showing results (1-10 of 10) with videos related to

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Proceedings of the Royal Society of Medicine|October 5, 2010
Transient Choreo-athetosis Following Hypernatræmia [Summary]T P Mann
Postgraduate Medical Journal|February 12, 2011
Sudden Death in Infancy: Royal Alexandra Hospital for Sick Children, BrightonT P Mann
Archives of Disease in Childhood|February 1, 1988
Noonan's syndrome and neurofibromatosisT P Mann
British Medical Journal|August 27, 2010
Finger-tip Necrosis in the Newly Born: A Hazard of Wearing MittensT P Mann
Proceedings of the Royal Society of Medicine|December 1, 1970
Chronic granulomatous diseaseT P Mann
Lancet (London, England)|May 6, 1972
Familial rectal painT P Mann, J E Cree
Archives of Disease in Childhood|August 1, 1971
Hereditary galactokinase deficiencyJ G Cook, N A Don, T P Mann
Postgraduate Medical Journal|March 1, 1976
GM1-generalized gangliosidosis variant with cardiomegalyP F Benson, A Barbarik, S P Brown, et al.
Proceedings of the Royal Society of Medicine|May 1, 1975
Chediak-Higashi syndromeJ E Cree, T P Mann, A D Webster, et al.
Archives of Disease in Childhood|February 1, 1972
Substrate induction of galactokinase in cultured fibroblasts from subjects heterozygous and homozygous for galactokinase deficiencyF Zacchello, P F Benson, P Croll, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Proceedings of the Royal Society of Medicine|October 5, 2010
Transient Choreo-athetosis Following Hypernatræmia [Summary]T P Mann
Postgraduate Medical Journal|February 12, 2011
Sudden Death in Infancy: Royal Alexandra Hospital for Sick Children, BrightonT P Mann
Archives of Disease in Childhood|February 1, 1988
Noonan's syndrome and neurofibromatosisT P Mann
British Medical Journal|August 27, 2010
Finger-tip Necrosis in the Newly Born: A Hazard of Wearing MittensT P Mann
Proceedings of the Royal Society of Medicine|December 1, 1970
Chronic granulomatous diseaseT P Mann
Lancet (London, England)|May 6, 1972
Familial rectal painT P Mann, J E Cree
Archives of Disease in Childhood|August 1, 1971
Hereditary galactokinase deficiencyJ G Cook, N A Don, T P Mann
Postgraduate Medical Journal|March 1, 1976
GM1-generalized gangliosidosis variant with cardiomegalyP F Benson, A Barbarik, S P Brown, et al.
Proceedings of the Royal Society of Medicine|May 1, 1975
Chediak-Higashi syndromeJ E Cree, T P Mann, A D Webster, et al.
Archives of Disease in Childhood|February 1, 1972
Substrate induction of galactokinase in cultured fibroblasts from subjects heterozygous and homozygous for galactokinase deficiencyF Zacchello, P F Benson, P Croll, et al.
Pageof 1