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P Aula

Showing results (51-60 of 161) with videos related to

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The Biochemical Journal|August 15, 1989
Isolation of a human hepatic 60 kDa aspartylglucosaminidase consisting of three non-identical polypeptidesM Baumann, L Peltonen, P Aula, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 13, 2003
Free sialic acid storage (Salla) disease in SwedenA Erikson, N Aula, P Aula, et al.
Hereditas|April 28, 2000
Origin of Finnish mutations causing aspartylglucosaminuriaS Valkonen, M Hietala, M L Savontaus, et al.
Clinical Genetics|February 1, 1990
Prenatal diagnosis in Pelizaeus-Merzbacher disease using RFLP analysisJ Mäenpää, E Lindahl, P Aula, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 15, 1976
Enzymatic determination of urinary aspartylglycosylamine: a rapid and sensitive-method to detect aspartylclycosylaminuria (AGU)K Sugahara, K Nishimura, P Aula, et al.
Clinical Genetics|January 1, 1973
Aspartylglucosaminuria: deficiency of aspartylglucosaminidase in cultured fibroblasts of patients and their heterozygous parentsP Aula, V Näntö, M L Laipio, et al.
American Journal of Medical Genetics|October 1, 1984
Prenatal diagnosis and fetal pathology of aspartylglucosaminuriaP Aula, J Rapola, H von Koskull, et al.
Clinical Genetics|June 1, 1978
Incomplete prenatal diagnosis of G-trisomy mosaicismK Simola, P Aula, M Ryynänen, et al.
FEBS Letters|October 15, 1976
Characterization of a mannose-containing glycoasparagine isolated from urine of a patient with aspartylglycosylaminuria (AGU)M Akasaki, K Sugahara, I Funakoshi, et al.
Lancet (London, England)|November 4, 1978
Prenatal screening for congenital nephrosisM Ryynänen, O Castren, J Rapola, et al.
Pageof 17

Showing results (51-60 of 161) with videos related to

Sort By:
Pageof 17
The Biochemical Journal|August 15, 1989
Isolation of a human hepatic 60 kDa aspartylglucosaminidase consisting of three non-identical polypeptidesM Baumann, L Peltonen, P Aula, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 13, 2003
Free sialic acid storage (Salla) disease in SwedenA Erikson, N Aula, P Aula, et al.
Hereditas|April 28, 2000
Origin of Finnish mutations causing aspartylglucosaminuriaS Valkonen, M Hietala, M L Savontaus, et al.
Clinical Genetics|February 1, 1990
Prenatal diagnosis in Pelizaeus-Merzbacher disease using RFLP analysisJ Mäenpää, E Lindahl, P Aula, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 15, 1976
Enzymatic determination of urinary aspartylglycosylamine: a rapid and sensitive-method to detect aspartylclycosylaminuria (AGU)K Sugahara, K Nishimura, P Aula, et al.
Clinical Genetics|January 1, 1973
Aspartylglucosaminuria: deficiency of aspartylglucosaminidase in cultured fibroblasts of patients and their heterozygous parentsP Aula, V Näntö, M L Laipio, et al.
American Journal of Medical Genetics|October 1, 1984
Prenatal diagnosis and fetal pathology of aspartylglucosaminuriaP Aula, J Rapola, H von Koskull, et al.
Clinical Genetics|June 1, 1978
Incomplete prenatal diagnosis of G-trisomy mosaicismK Simola, P Aula, M Ryynänen, et al.
FEBS Letters|October 15, 1976
Characterization of a mannose-containing glycoasparagine isolated from urine of a patient with aspartylglycosylaminuria (AGU)M Akasaki, K Sugahara, I Funakoshi, et al.
Lancet (London, England)|November 4, 1978
Prenatal screening for congenital nephrosisM Ryynänen, O Castren, J Rapola, et al.
Pageof 17