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H R WIEDEMANN

Showing results (141-150 of 151) with videos related to

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Journal of Neurochemistry|December 1, 1973
Brain lipids of a case of juvenile Niemann-Pick diseaseH B Tjiong, P N Seng, H Debuch, et al.
Advances in Experimental Medicine and Biology|January 1, 1972
Drug usage and fetal development: preliminary evaluations of a prospective investigationK H Degenhardt, H Kerken, K Knörr, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1974
Achondrogenesis within the scope of connately manifested generalized skeletal dysplasiasH R Wiedemann, W Remagen, H A Hienz, et al.
American Journal of Medical Genetics|June 1, 1994
Reduced renal excretion of uric acid in the hirsutism-skeletal dysplasia--mental retardation syndromeO Oster, H R Wiedemann, I A Duley, et al.
Helvetica Paediatrica Acta|October 1, 1970
Mucopolysaccharidosis VI (Maroteaux-Lamy's disease)J W Spranger, F Koch, V A McKusick, et al.
Journal of Medical Genetics|February 25, 1998
Is p57KIP2 mutation a common mechanism for Beckwith-Wiedemann syndrome or somatic overgrowth?K Okamoto, I M Morison, A E Reeve, et al.
European Journal of Pediatrics|March 1, 1983
The proteus syndrome. Partial gigantism of the hands and/or feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly or other skull anomalies and possible accelerated growth and visceral affectionsH R Wiedemann, G R Burgio, P Aldenhoff, et al.
American Journal of Medical Genetics|October 16, 1996
Blepharo-cheilo-dontic (BCD) syndromeR J Gorlin, H Zellweger, M W Curtis, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1972
[An infantile-juvenile, subchronically progressive lipoidosis of the sphingomyelinoses (Niemann-Pick) form--a new type? Clinical, pathohistological, electron microscopic and biochemical studies]H R Wiedemann, H Debuch, K Lennert, et al.
American Journal of Medical Genetics|January 1, 1981
Further delineation of the C (trigonocephaly) syndromeR M Antley, D S Hwang, W Theopold, et al.
Pageof 16

Showing results (141-150 of 151) with videos related to

Sort By:
Pageof 16
Journal of Neurochemistry|December 1, 1973
Brain lipids of a case of juvenile Niemann-Pick diseaseH B Tjiong, P N Seng, H Debuch, et al.
Advances in Experimental Medicine and Biology|January 1, 1972
Drug usage and fetal development: preliminary evaluations of a prospective investigationK H Degenhardt, H Kerken, K Knörr, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1974
Achondrogenesis within the scope of connately manifested generalized skeletal dysplasiasH R Wiedemann, W Remagen, H A Hienz, et al.
American Journal of Medical Genetics|June 1, 1994
Reduced renal excretion of uric acid in the hirsutism-skeletal dysplasia--mental retardation syndromeO Oster, H R Wiedemann, I A Duley, et al.
Helvetica Paediatrica Acta|October 1, 1970
Mucopolysaccharidosis VI (Maroteaux-Lamy's disease)J W Spranger, F Koch, V A McKusick, et al.
Journal of Medical Genetics|February 25, 1998
Is p57KIP2 mutation a common mechanism for Beckwith-Wiedemann syndrome or somatic overgrowth?K Okamoto, I M Morison, A E Reeve, et al.
European Journal of Pediatrics|March 1, 1983
The proteus syndrome. Partial gigantism of the hands and/or feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly or other skull anomalies and possible accelerated growth and visceral affectionsH R Wiedemann, G R Burgio, P Aldenhoff, et al.
American Journal of Medical Genetics|October 16, 1996
Blepharo-cheilo-dontic (BCD) syndromeR J Gorlin, H Zellweger, M W Curtis, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1972
[An infantile-juvenile, subchronically progressive lipoidosis of the sphingomyelinoses (Niemann-Pick) form--a new type? Clinical, pathohistological, electron microscopic and biochemical studies]H R Wiedemann, H Debuch, K Lennert, et al.
American Journal of Medical Genetics|January 1, 1981
Further delineation of the C (trigonocephaly) syndromeR M Antley, D S Hwang, W Theopold, et al.
Pageof 16