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Results of search for 'au:"Germain, D P"', page 2 of 3
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Authors
Baillet, A
Benistan, K
Bonfils, P
Boutouyrie, P
Caillaud, C
Carlier, R Y
Caudron, E
Chaminade, P
Colas, F
Eng, C M
Gaudin, K
Germain, D P
Germain, D-P
Grunfeld, J P
Jabbour, F
Jeunemaitre, X
Lacombe, D
Laloux, B
Laurent, S
Waldek, S
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Adolescent
Adult
Age Factors
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Child
DNA Mutational Analysis
Fabry Disease
Female
Gaucher Disease
Humans
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Middle Aged
Mutation
alpha-Galactosidase
complications
diagnosis
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21.
X-linked inheritance and its implication in the diagnosis and management of female patients in Fabry disease.
[electronic resource]
by
Germain, D P
Benistan, K
Angelova, L
Producer:
20110607
In:
La Revue de medecine interne
vol. 31 Suppl 2
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22.
[Fabry disease: enzymatic screening using dried blood spots on filter paper].
[electronic resource]
by
Caudron, E
Germain, D P
Prognon, P
Producer:
20110607
In:
La Revue de medecine interne
vol. 31 Suppl 2
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23.
Eighth International Symposium on Lysosomal Storage Diseases.
[electronic resource]
by
Mehta, A B
Germain, D P
Martin, R
Producer:
20100305
In:
International journal of clinical pharmacology and therapeutics
vol. 47 Suppl 1
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24.
[Azoospermia as a new feature of Fabry disease].
[electronic resource]
by
Lacombe, D
Germain, D P
Papaxanthos-Roche, A
Producer:
20110607
In:
La Revue de medecine interne
vol. 31 Suppl 2
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25.
Homozygosity for the R1268Q mutation in MRP6, the pseudoxanthoma elasticum gene, is not disease-causing.
[electronic resource]
by
Germain, D P
Perdu, J
Remones, V
Jeunemaitre, X
Producer:
20000824
In:
Biochemical and biophysical research communications
vol. 274
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26.
Identification of two polymorphisms (c189G>C; c190T>C) in exon 2 of the human MRP6 gene (ABCC6) by screening of Pseudoxanthoma elasticum patients: possible sequence correction?
[electronic resource]
by
Germain, D P
Remones, V
Perdu, J
Jeunemaitre, X
Producer:
20001121
In:
Human mutation
vol. 16
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27.
[Vestibular and cochlear manifestations in Fabry's disease].
[electronic resource]
by
Malinvaud, D
Germain, D P
Benistan, K
Bonfils, P
Producer:
20110607
In:
La Revue de medecine interne
vol. 31 Suppl 2
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28.
Mutation analysis of the acid beta-glucosidase gene in a patient with type 3 Gaucher disease and neutralizing antibody to alglucerase.
[electronic resource]
by
Germain, D P
Kaneski, C R
Brady, R O
Producer:
20011214
In:
Mutation research
vol. 483
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29.
[The cochlea in Fabry disease: a sensorineural hearing loss model of vascular origin?].
[electronic resource]
by
Malinvaud, D
Avan, P
Germain, D P
Benistan, K
Bonfils, P
Producer:
20060912
In:
La Revue de medecine interne
vol. 27
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30.
Exhaustive screening of the acid beta-glucosidase gene, by fluorescence-assisted mismatch analysis using universal primers: mutation profile and genotype/phenotype correlations in Gaucher disease.
[electronic resource]
by
Germain, D P
Puech, J P
Caillaud, C
Kahn, A
Poenaru, L
Producer:
19981224
In:
American journal of human genetics
vol. 63
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31.
Optimisation of the separation of four major neutral glycosphingolipids: application to a rapid and simple detection of urinary globotriaosylceramide in Fabry disease.
[electronic resource]
by
Roy, S
Gaudin, K
Germain, D P
Baillet, A
Prognon, P
Chaminade, P
Producer:
20050121
In:
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
vol. 805
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32.
Non-invasive evaluation of arterial involvement in patients affected with Fabry disease.
[electronic resource]
by
Boutouyrie, P
Laurent, S
Laloux, B
Lidove, O
Grunfeld, J P
Germain, D P
Producer:
20020110
In:
Journal of medical genetics
vol. 38
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33.
Arterial remodelling in Fabry disease.
[electronic resource]
by
Boutouyrie, P
Laurent, S
Laloux, B
Lidove, O
Grunfeld, J P
Germain, D P
Producer:
20030523
In:
Acta paediatrica (Oslo, Norway : 1992). Supplement
vol. 91
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34.
[Imaging mass spectrometry: a new tool for the analysis of skin biopsy. Application in Fabry's disease].
[electronic resource]
by
Roy, S
Touboul, D
Brunelle, A
Germain, D-P
Prognon, P
Laprévote, O
Chaminade, P
Producer:
20061206
In:
Annales pharmaceutiques francaises
vol. 64
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35.
Identification of a novel de novo mutation (G373D) in the alpha-galactosidase A gene (GLA) in a patient affected with Fabry disease.
[electronic resource]
by
Germain, D P
Salard, D
Fellmann, F
Azibi, K
Caillaud, C
Bernard, M C
Poenaru, L
Producer:
20010816
In:
Human mutation
vol. 17
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36.
[Niemann-Pick disease type B identified following an episode of bronchopneumonia].
[electronic resource]
by
Hervé, A
Marchand-Adam, S
Fabre, A
Debray, M-P
Germain, D-P
Crestani, B
Aubier, M
Producer:
20081216
In:
Revue des maladies respiratoires
vol. 25
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37.
Compressibility of the carotid artery in patients with pseudoxanthoma elasticum.
[electronic resource]
by
Boutouyrie, P
Germain, D P
Tropeano, A I
Laloux, B
Carenzi, F
Zidi, M
Jeunemaitre, X
Laurent, S
Producer:
20011207
In:
Hypertension (Dallas, Tex. : 1979)
vol. 38
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38.
Liquid chromatography on porous graphitic carbon with atmospheric pressure photoionization mass spectrometry and tandem mass spectrometry for the analysis of glycosphingolipids.
[electronic resource]
by
Roy, S
Delobel, A
Gaudin, K
Touboul, D
Germain, D P
Baillet, A
Prognon, P
Laprévote, O
Chaminade, P
Producer:
20060727
In:
Journal of chromatography. A
vol. 1117
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39.
[Neurological aspects of Fabry's disease].
[electronic resource]
by
Clavelou, P
Besson, G
Elziere, C
Ferrier, A
Pinard, J-M
Hermier, M
Artigou, J Y
Germain, D P
Producer:
20060928
In:
Revue neurologique
vol. 162
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40.
Basilar Artery Changes in Fabry Disease.
[electronic resource]
by
Manara, R
Carlier, R Y
Righetto, S
Citton, V
Locatelli, G
Colas, F
Ermani, M
Germain, D P
Burlina, A
Producer:
20171018
In:
AJNR. American journal of neuroradiology
vol. 38
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