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Results of search for 'su:"Zellweger Syndrome"', page 2 of 31
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Authors
Barth, P G
Fujiki, Y
Gärtner, J
Hashimoto, T
Jakobs, C
Kondo, N
Mannaerts, G P
Moser, A B
Moser, H W
Orii, T
Poll-The, Bwee Tien
Poulos, A
Schutgens, R B
Shimozawa, N
Suzuki, Y
Tager, J M
Tsukamoto, T
Wanders, R J
Wanders, Ronald J A
Waterham, Hans R
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Adrenoleukodystrophy
Animals
Fatty Acids
Female
Fibroblasts
Humans
Infant
Infant, Newborn
Liver
Male
Membrane Proteins
Microbodies
Mutation
Peroxisomal Disorders
Peroxisomes
Zellweger Syndrome
diagnosis
enzymology
genetics
metabolism
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21.
Intestinal lymphangiectasia in a patient with Zellweger cerebrohepatorenal syndrome.
[electronic resource]
by
Erdem, G
Oran, O
Kotiloğlu, E
Kale, G
Topçu, M
Renda, Y
Producer:
19960129
In:
American journal of medical genetics
vol. 58
Online resources:
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22.
[Peroxisomal disorders (Zellweger syndrome)].
[electronic resource]
by
Owada, M
Producer:
19971114
In:
Ryoikibetsu shokogun shirizu
no. 17 Pt 2
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23.
Defective oxidation of hydroxyeicosatetraenoic acids in the liver of patients with Zellweger syndrome.
[electronic resource]
by
Mayatepek, E
Wanders, R J
Producer:
19981104
In:
Journal of inherited metabolic disease
vol. 21
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24.
Defective degradation of leukotrienes in peroxisomal-deficient human hepatocytes.
[electronic resource]
by
Mayatepek, E
Tiepelmann, B
Producer:
19961125
In:
Biochemical and biophysical research communications
vol. 227
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25.
[Case report of the clinico-biochemical diagnosis of the peroxisomal disease syndrome of Zellweger].
[electronic resource]
by
Klánová, M
Kozich, V
Pehal, F
Producer:
19901005
In:
Ceskoslovenska pediatrie
vol. 45
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26.
[A novel mutation in PEX 26 gene in Zellweger syndrome: a case report].
[electronic resource]
by
Ben Turkia, Hadhami
Yangui, Mohamed
Azzouz, Hatem
Ben Chehida, Amal
Ben Abelaziz, Rim
Abdelmoula, Mohamed Slim
Nasrallah, Fehmi
Kaabachi, Naziha
Wanders, Ronald
Tebib, Neji
Ben Dridi, Marie Françoise
Producer:
20110801
In:
La Tunisie medicale
vol. 89
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27.
Impaired DNA synthesis in dermal fibroblasts from Zellweger syndrome patients.
[electronic resource]
by
Dhaunsi, G S
Rahbeeni, Z
al-Essa, M
Ozand, P T
Producer:
19980611
In:
Journal of inherited metabolic disease
vol. 21
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28.
Child neurology: Zellweger syndrome.
[electronic resource]
by
Lee, Paul R
Raymond, Gerald V
Producer:
20130708
In:
Neurology
vol. 80
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29.
[Introduction to peroxisomal disorders].
[electronic resource]
by
Orii, T
Producer:
19980925
In:
Ryoikibetsu shokogun shirizu
no. 19 Pt 2
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30.
Peroxisomal diseases: a microscopist looks through the retrospectroscope.
[electronic resource]
by
Goldfischer, S
Producer:
19970210
In:
Annals of the New York Academy of Sciences
vol. 804
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31.
Chondrodisplasia Punctata of Hip Joints on Routine Radiography Provided a Diagnostic Clue of Zellweger Syndrome.
[electronic resource]
by
Kitaoka, Hiroki
Shitara, Yoshihiko
Kondo, Utako
Kushima, Reiko
Omori, Isaku
Producer:
20200107
In:
Pediatric neurology
vol. 98
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32.
Postnatal diagnosis of peroxisomal disorders: a biochemical approach.
[electronic resource]
by
Wanders, R J
Schutgens, R B
Barth, P G
Tager, J M
van den Bosch, H
Producer:
19930709
In:
Biochimie
vol. 75
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33.
Clinical and biochemical characteristics of peroxisomal disorders: an update.
[electronic resource]
by
Wanders, R J
Barth, P G
Schutgens, R B
Tager, J M
Producer:
19941227
In:
European journal of pediatrics
vol. 153
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34.
Characteristic urine organic acid profile in peroxisomal biogenesis disorders.
[electronic resource]
by
Korman, S H
Mandel, H
Gutman, A
Producer:
20001116
In:
Journal of inherited metabolic disease
vol. 23
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35.
A specific method for determination of peroxisomal beta-oxidation activity in cultured human skin fibroblasts using a specific substrate, C9: a possible application for screening of peroxisomal disorders.
[electronic resource]
by
Suzuki, H
Yamada, J
Watanabe, T
Suga, T
Producer:
19920702
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 207
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36.
Peroxisomal diseases.
[electronic resource]
by
Goldfischer, S L
Producer:
19890519
In:
Progress in clinical and biological research
vol. 282
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37.
[Peroxisomal diseases: an analysis of ferritin levels in Zellweger's cerebrohepatorenal syndrome].
[electronic resource]
by
Carrascosa-Romero, M C
Vidal-Company, A
Gil-Pons, E
Perez-Pardo, A
Marco-Giner, J
Tebar-Gil, R
Producer:
20080915
In:
Revista de neurologia
vol. 46
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38.
High prevalence of primary adrenal insufficiency in Zellweger spectrum disorders.
[electronic resource]
by
Berendse, Kevin
Engelen, Marc
Linthorst, Gabor E
van Trotsenburg, A S Paul
Poll-The, Bwee Tien
Producer:
20150330
In:
Orphanet journal of rare diseases
vol. 9
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39.
Oral Cholic Acid Is Efficacious and Well Tolerated in Patients With Bile Acid Synthesis and Zellweger Spectrum Disorders.
[electronic resource]
by
Heubi, James E
Bove, Kevin E
Setchell, Kenneth D R
Producer:
20190226
In:
Journal of pediatric gastroenterology and nutrition
vol. 66
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40.
Role of peroxisomes in the degradation of prostaglandins.
[electronic resource]
by
Diczfalusy, U G
Alexson, S E
Producer:
19921218
In:
Progress in clinical and biological research
vol. 375
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