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R. M. Gardiner

Veröffentlichungen von R. M. Gardiner zu Santavuori, Pirkko ->
weitere Veröffentlichungen von R. M. Gardiner:
Cephalotaxine analogs: stereospecific synthesis of spiro-fused 3-benzazepine and 1,3-benzodiazepine derivatives (1990)
Stereoselective Synthesis of 1,2-13C2-l-Fucose, 1,2-13C2-Fucono-γ-lactone and 1,2-13C2-Fucono-γ-lactol from Non-Sugar Starting Material (2005)
Benign Childhood Epilepsy with Centrotemporal Spikes and the Focal Sharp Wave Trait is not Linked to the Fragile X Region (1993)
Evidence for intramolecular carbon-hydrogen bond activation and the formation of a tucked-in complex of hexamethylbenzene at a tantalum(III) center (1989)
Stable tertiary phosphine adducts of alane (1992)
Transport of amino acids across the blood-brain barrier: Implications for treatment of maternal phenylketonuria (1990)
Genetic analysis of Batten disease (1993)
Impact of our understanding of the genetic aetiology of epilepsy (2000)
The molecular genetic basis of the neuronal ceroid lipofuscinoses (2000)
Cerebral ammonia production during hypoglycaemia in the newborn calf (1979)
Potassium transfer from brain to blood during sustained hyponatraemia in the newborn calf (1980)
Peroxidase isoenzymes of the Avena coleoptile (1974)
Peroxidase changes during the cessation of elongation in Pisum sativum stems (1974)
Influence of vitamin B"1"2 on the urinary excretion of folic acid metabolites by the rat (1960)
The Evolution Of Turbulence Across A Forest Edge (1997)
Veröffentlichungen zu Santavuori, Pirkko
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1
Haltia, Matti, Rapola, Juhani, ... Infantile type of so-called neuronal ceroid-lipofuscinosis
in: Acta neuropathologica , ISSN 1432-0533, Vol. 26 (2. 1973), p. 157-170
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1973
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2
Savukoski, Minna, Klockars, Tuomas, ... CLN5, a novel gene encoding a putative transmembrane protein mutatedin Finnish variant late infantile neuronal ceroid lipofuscinosis
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 19, No. 3 (1998), p. 286-288
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1998
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3
Vesa, Jouni, Hellsten, Elina, ... Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 376, No. 6541 (1995), p. 584-587
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1995
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4
Gardiner, R. M.., Järvelä, Irma E.., ... Strategy for Mutation Detection in CLN3: Characterisation of Two Finnish Mutations
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 28, No. 01 (2. 1997), p. 15-17
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1997
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5
Gardiner, R. M.., Järvelä, Irma E.., ... Strategy for Mutation Detection in CLN3: Characterisation of Two Finnish Mutations
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 28, No. 01 (2. 1997), p. 15-17
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1997
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6
Munroe, Patricia B.., O'Rawe, Angela M.., ... Strategy for Mutation Detection in CLN3: Characterisation of Two Finnish Mutations
in: Neuropediatrics. - Stuttgart [u.a.] : Thieme, ISSN 1439-1899, Vol. 28, No. 01 (1997), p. 15-17
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1997