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Annals of the New York Academy of Sciences
|
January 1, 1987
A congenital myasthenic disorder with paucity of secondary synaptic clefts: deficiency and altered distribution of acetylcholine receptors
L M Smit, H Veldman, F G Jennekens, et al.
Muscle & Nerve
|
April 1, 1988
A myasthenic syndrome with congenital paucity of secondary synaptic clefts: CPSC syndrome
L M Smit, G Hageman, H Veldman, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
May 24, 2001
[Intracranial hemorrhages in infants: child abuse or a congenital coagulation disorder?]
K P Bach, A Y Schouten-van Meeteren, L M Smit, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
February 11, 2000
[Children with stumbling gait due to acute spinal cord compression]
M J Koppe, T G de Haas, W J van Ouwerkerk, et al.
Clinical Genetics
|
August 1, 1988
Karyotyping urine sediment cells confirms trisomy 12 mosaicism detected at amniocentesis
N J Leschot, E J Wilmsen-Linders, H P van Geijn, et al.
European Journal of Pediatrics
|
February 1, 1991
The first prenatal diagnosis of dihydropyrimidine dehydrogenase deficiency
C Jakobs, F Stellaard, L M Smit, et al.
European Journal of Pediatrics
|
February 1, 1990
A new case of hyperargininaemia: neurological and biochemical findings prior to and during dietary treatment
M Brockstedt, L M Smit, A J de Grauw, et al.
European Journal of Pediatrics
|
January 1, 1991
Infantile isolated sulphite oxidase deficiency: report of a case with negative sulphite test and normal sulphate excretion
J M van der Klei-van Moorsel, L M Smit, M Brockstedt, et al.
Neuropediatrics
|
August 1, 1990
Acute hemiparesis as the presenting sign in a heterozygote for ornithine transcarbamylase deficiency
T J de Grauw, L M Smit, M Brockstedt, et al.
Journal of the Neurological Sciences
|
March 1, 1990
Morphological changes in the human end plate with age
J H Wokke, F G Jennekens, C J van den Oord, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 40) with videos related to
Sort By:
Page
of 4
Annals of the New York Academy of Sciences
|
January 1, 1987
A congenital myasthenic disorder with paucity of secondary synaptic clefts: deficiency and altered distribution of acetylcholine receptors
L M Smit, H Veldman, F G Jennekens, et al.
Muscle & Nerve
|
April 1, 1988
A myasthenic syndrome with congenital paucity of secondary synaptic clefts: CPSC syndrome
L M Smit, G Hageman, H Veldman, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
May 24, 2001
[Intracranial hemorrhages in infants: child abuse or a congenital coagulation disorder?]
K P Bach, A Y Schouten-van Meeteren, L M Smit, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
February 11, 2000
[Children with stumbling gait due to acute spinal cord compression]
M J Koppe, T G de Haas, W J van Ouwerkerk, et al.
Clinical Genetics
|
August 1, 1988
Karyotyping urine sediment cells confirms trisomy 12 mosaicism detected at amniocentesis
N J Leschot, E J Wilmsen-Linders, H P van Geijn, et al.
European Journal of Pediatrics
|
February 1, 1991
The first prenatal diagnosis of dihydropyrimidine dehydrogenase deficiency
C Jakobs, F Stellaard, L M Smit, et al.
European Journal of Pediatrics
|
February 1, 1990
A new case of hyperargininaemia: neurological and biochemical findings prior to and during dietary treatment
M Brockstedt, L M Smit, A J de Grauw, et al.
European Journal of Pediatrics
|
January 1, 1991
Infantile isolated sulphite oxidase deficiency: report of a case with negative sulphite test and normal sulphate excretion
J M van der Klei-van Moorsel, L M Smit, M Brockstedt, et al.
Neuropediatrics
|
August 1, 1990
Acute hemiparesis as the presenting sign in a heterozygote for ornithine transcarbamylase deficiency
T J de Grauw, L M Smit, M Brockstedt, et al.
Journal of the Neurological Sciences
|
March 1, 1990
Morphological changes in the human end plate with age
J H Wokke, F G Jennekens, C J van den Oord, et al.
Page
of 4