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S Similä

Showing results (71-80 of 100) with videos related to

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Pediatrics|June 1, 1980
Failure of strychnine treatment during the neonatal period in three Finnish children with nonketotic hyperglycinemiaL von Wendt, S Similä, A L Saukkonen, et al.
Annals of Clinical Research|August 1, 1980
Serum bile acid concentrations in the course of benign recurrent intrahepatic cholestasisK Finni, S Similä, S Heikura, et al.
Journal of Inherited Metabolic Disease|January 14, 1998
L-3-hydroxyacyl-CoA dehydrogenase deficiency: two cases with pigmentary retinopathyJ Uusimaa, L Vainionpää, S Similä, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1971
Fatal familial steatosis of the liver and kidney in two siblingsO Räsänen, M Korhonen, S Similä, et al.
Acta Paediatrica Scandinavica|September 1, 1980
Cholic acid and chenodeoxycholic acid concentrations in serum during infancy and childhoodS Heikura, S Similä, K Finni, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1982
[Methylmalonic aciduria]S Similä, A Ruokonen, A Palotie, et al.
Developmental Medicine and Child Neurology|June 1, 1990
Development of bowel and bladder control in the mentally retardedL von Wendt, S Similä, P Niskanen, et al.
Archives of Disease in Childhood|August 1, 1978
Familial syndrome with panhypopituitarism, hypoplasia of the hypophysis, and poorly developed sella turcicaP Sipponen, S Similä, Y Collan, et al.
Acta Paediatrica Scandinavica|March 1, 1980
An arthropathic form of osteogenesis imperfectaR Penttinen, E Sipola, K Kouvalainen, et al.
Annals of Clinical Research|January 1, 1983
Propionic acidaemia. First case in the Finnish populationL von Wendt, S Similä, J Ruostesuo, et al.
Pageof 10

Showing results (71-80 of 100) with videos related to

Sort By:
Pageof 10
Pediatrics|June 1, 1980
Failure of strychnine treatment during the neonatal period in three Finnish children with nonketotic hyperglycinemiaL von Wendt, S Similä, A L Saukkonen, et al.
Annals of Clinical Research|August 1, 1980
Serum bile acid concentrations in the course of benign recurrent intrahepatic cholestasisK Finni, S Similä, S Heikura, et al.
Journal of Inherited Metabolic Disease|January 14, 1998
L-3-hydroxyacyl-CoA dehydrogenase deficiency: two cases with pigmentary retinopathyJ Uusimaa, L Vainionpää, S Similä, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1971
Fatal familial steatosis of the liver and kidney in two siblingsO Räsänen, M Korhonen, S Similä, et al.
Acta Paediatrica Scandinavica|September 1, 1980
Cholic acid and chenodeoxycholic acid concentrations in serum during infancy and childhoodS Heikura, S Similä, K Finni, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1982
[Methylmalonic aciduria]S Similä, A Ruokonen, A Palotie, et al.
Developmental Medicine and Child Neurology|June 1, 1990
Development of bowel and bladder control in the mentally retardedL von Wendt, S Similä, P Niskanen, et al.
Archives of Disease in Childhood|August 1, 1978
Familial syndrome with panhypopituitarism, hypoplasia of the hypophysis, and poorly developed sella turcicaP Sipponen, S Similä, Y Collan, et al.
Acta Paediatrica Scandinavica|March 1, 1980
An arthropathic form of osteogenesis imperfectaR Penttinen, E Sipola, K Kouvalainen, et al.
Annals of Clinical Research|January 1, 1983
Propionic acidaemia. First case in the Finnish populationL von Wendt, S Similä, J Ruostesuo, et al.
Pageof 10