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P Strømme

Showing results (21-30 of 33) with videos related to

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European Urology|January 1, 1987
Unilateral vesicoureteral reflux in children. study on urine specific gravity, osmolality, beta-2-microglobulin and lactoferrinT J Gutteberg, P Strømme, J Saebø-Larsen, et al.
Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery|January 1, 1993
Cleft lip and palate, scoliosis, skeletal and cardiac malformations and other dysmorphic features in a child. Case reportP Strømme, J Knudtzon, J Westvik, et al.
Logopedics, Phoniatrics, Vocology|February 1, 2011
Learning disabilities and language pathology in patients with galactosemiaR K Rasmussen, A B Andreassen, P Strømme, et al.
AJNR. American Journal of Neuroradiology|May 1, 1991
Bilateral arachnoid cysts of the temporal fossa in four children with glutaric aciduria type IJ K Hald, P H Nakstad, O H Skjeldal, et al.
Clinical Genetics|July 1, 1995
Atypical methylmalonic aciduria with progressive encephalopathy, microcephaly and cataract in two siblings--a new recessive syndrome?P Strømme, O Stokke, E Jellum, et al.
Pediatric Neurology|February 1, 1997
Encephaloneuropathy with lysosomal zebra bodies and GM2 ganglioside storageP Strømme, J E Månsson, H Scott, et al.
Journal of Medical Genetics|November 14, 1997
Macrocephaly, epilepsy, autism, dysmorphic features, and mental retardation in two sisters: a new autosomal recessive syndrome?K H Orstavik, P Strømme, J Ek, et al.
Journal of Medical Genetics|June 3, 1999
X linked mental retardation and infantile spasms in a family: new clinical data and linkage to Xp11.4-Xp22.11P Strømme, K Sundet, C Mørk, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 19, 2009
Parental consanguinity is associated with a seven-fold increased risk of progressive encephalopathy: a cohort study from Oslo, NorwayP Strømme, P Suren, O J Kanavin, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan-McDermid syndrome and hypergonadotropic hypogonadismD Misceo, O K Rødningen, T Barøy, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
European Urology|January 1, 1987
Unilateral vesicoureteral reflux in children. study on urine specific gravity, osmolality, beta-2-microglobulin and lactoferrinT J Gutteberg, P Strømme, J Saebø-Larsen, et al.
Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery|January 1, 1993
Cleft lip and palate, scoliosis, skeletal and cardiac malformations and other dysmorphic features in a child. Case reportP Strømme, J Knudtzon, J Westvik, et al.
Logopedics, Phoniatrics, Vocology|February 1, 2011
Learning disabilities and language pathology in patients with galactosemiaR K Rasmussen, A B Andreassen, P Strømme, et al.
AJNR. American Journal of Neuroradiology|May 1, 1991
Bilateral arachnoid cysts of the temporal fossa in four children with glutaric aciduria type IJ K Hald, P H Nakstad, O H Skjeldal, et al.
Clinical Genetics|July 1, 1995
Atypical methylmalonic aciduria with progressive encephalopathy, microcephaly and cataract in two siblings--a new recessive syndrome?P Strømme, O Stokke, E Jellum, et al.
Pediatric Neurology|February 1, 1997
Encephaloneuropathy with lysosomal zebra bodies and GM2 ganglioside storageP Strømme, J E Månsson, H Scott, et al.
Journal of Medical Genetics|November 14, 1997
Macrocephaly, epilepsy, autism, dysmorphic features, and mental retardation in two sisters: a new autosomal recessive syndrome?K H Orstavik, P Strømme, J Ek, et al.
Journal of Medical Genetics|June 3, 1999
X linked mental retardation and infantile spasms in a family: new clinical data and linkage to Xp11.4-Xp22.11P Strømme, K Sundet, C Mørk, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 19, 2009
Parental consanguinity is associated with a seven-fold increased risk of progressive encephalopathy: a cohort study from Oslo, NorwayP Strømme, P Suren, O J Kanavin, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan-McDermid syndrome and hypergonadotropic hypogonadismD Misceo, O K Rødningen, T Barøy, et al.
Pageof 4