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Results of search for 'au:"PHILIPPART, M"', page 2 of 6
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Authors
Andermann, E
Andermann, F
Bateman, J B
Bayever, E
Bensaude, I
Borrone, C
CLARK, D B
Callahan, J W
Chugani, H T
Deberdt, R
Delbeke, M J
Della Cella, G
Durand, P
Hooft, C
Hull, A R
MENKES, J H
Martin, J J
Menkes, J H
PHILIPPART, M
Philippart, M
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Topics
Adolescent
Adult
Brain
Child
Child, Preschool
Diagnosis, Differential
Female
Glycolipids
Humans
Infant
Lipid Metabolism, Inborn Errors
Liver
Male
analysis
complications
diagnosis
enzymology
genetics
metabolism
pathology
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Your search returned 103 results.
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21.
Chemical induction of lysosomal storage.
[electronic resource]
by
Philippart, M
Kamensky, E
Producer:
19760823
In:
Advances in experimental medicine and biology
vol. 68
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22.
Neuronal ceroid-lipofuscinosis: late infantile form or juvenile form?
[electronic resource]
by
Philippart, M
Chugani, B
Producer:
19951113
In:
Brain & development
vol. 17
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23.
Cholestanol storage in the nervous system of two patients with cerebrotendinous xanthomatosis.
[electronic resource]
by
Menkes, J H
Philippart, M
Producer:
19690409
In:
Transactions of the American Neurological Association
vol. 93
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24.
Biochemical methods in the detection and diagnosis of metabolic diseases affecting the nervous system.
[electronic resource]
by
Menkes, J H
Philippart, M
Producer:
19671215
In:
Journal of the neurological sciences
vol. 2
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25.
Ocular features of the Hagberg-Santavuori syndrome.
[electronic resource]
by
Bateman, J B
Philippart, M
Producer:
19860917
In:
American journal of ophthalmology
vol. 102
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26.
Cerebrotendinous xanthomatosis: a generalized disorder of cholestanol metabolism.
[electronic resource]
by
Philippart, M
van Bogaert, L
Producer:
19700427
In:
Transactions of the American Neurological Association
vol. 94
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27.
[Unusual types of course of polyradiculitis with cerebrospinal fluid dissociation (Guillain-Barre type) (recurring and chronic forms). (Critical evaluation of corticosteroid therapy)].
[electronic resource]
by
MARTIN, J J
PHILIPPART, M
Producer:
19981101
In:
World neurology
vol. 3
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28.
Chondroitin-4-sulphate mucopolysaccharidosis--a new variant of Hurler's syndrome.
[electronic resource]
by
Philippart, M
Sugarman, G I
Producer:
19691127
In:
Lancet (London, England)
vol. 2
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29.
Multiple sclerosis in childhood.
[electronic resource]
by
Philippart, M
Curran, J G
Producer:
19930823
In:
Brain & development
vol. 15
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30.
Cholestanolosis (cerebrotendinous xanthomatosis). A follow-up study on the original family.
[electronic resource]
by
Philippart, M
Van Bogaert, L
Producer:
19700119
In:
Archives of neurology
vol. 21
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31.
Fabry's disease as an -galactosidosis: evidence for an -configuration in trihexosyl ceramide.
[electronic resource]
by
Bensaude, I
Callahan, J
Philippart, M
Producer:
19711014
In:
Biochemical and biophysical research communications
vol. 43
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32.
Neutral lipid storage with acid lipase deficiency: a new variant of Wolman's disease with features of the Senior syndrome.
[electronic resource]
by
Philippart, M
Durand, P
Borrone, C
Producer:
19830311
In:
Pediatric research
vol. 16
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33.
Fabry's disease with hypogammaglobulinemia and without angiokeratomas.
[electronic resource]
by
Urbain, G
Philippart, M
Peremans, J
Producer:
19690821
In:
Archives of internal medicine
vol. 124
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34.
Alpha-galactosidic configuration in ceramide trihexoside synthesized by rat spleen homogenate.
[electronic resource]
by
Bensaude, I
Philippart, M
Hildebrand, J
Producer:
19730208
In:
Biochemical medicine
vol. 6
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35.
Urinary glycolipids in Fabry's disease. Their examination in the detection of atypical variants and the pre-symptomatic state.
[electronic resource]
by
Philippart, M
Sarlieve, L
Manacorda, A
Producer:
19690319
In:
Pediatrics
vol. 43
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36.
Oral Delivery of Therapeutic Proteins and Peptides: An Overview of Current Technologies and Recommendations for Bridging from Approved Intravenous or Subcutaneous Administration to Novel Oral Regimens.
[electronic resource]
by
Philippart, M
Schmidt, J
Bittner, B
Producer:
20161213
In:
Drug research
vol. 66
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37.
Reversal of an inborn sphingolipidosis (Fabry's disease) by kidney transplantation.
[electronic resource]
by
Philippart, M
Franklin, S S
Gordon, A
Producer:
19730217
In:
Annals of internal medicine
vol. 77
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38.
Glycolipid alterations in Niemann-Pick disease (Crocker type C).
[electronic resource]
by
Philippart, M
Martin, L
Martin, J J
Producer:
19680807
In:
Neurology
vol. 18
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39.
[On 2 cases of Niemann-Pick disease. Chronic form with delayed neurologic involvement].
[electronic resource]
by
Jansseune, H
Philippart, M
Martin, J J
Producer:
19690205
In:
Acta paediatrica Belgica
vol. 21
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40.
Gelastic cataplexy in Niemann-Pick disease group C and related variants without generalized sphingomyelinase deficiency.
[electronic resource]
by
Philippart, M
Engel, J
Zimmerman, E G
Producer:
19831220
In:
Annals of neurology
vol. 14
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