The mechanism of arrest of neuronal migration in the Zellweger malformation: An hypothesis based upon cytoarchitectonic analysis
Evrard, P., Caviness, V. S., Prats-Vinas, J., Lyon, G.·1978·Acta Neuropathologica
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- Wiring, dysmorphogenesis and epilepsy: A hypothesisSanjay M. Sisodiya · 1995 · Seizure
- Intrauterine multisystem atrophy in siblings: A new genetic syndrome?Maie Kaarsoo Herrick, Aaron M. Strefling, Henry Urich · 1983 · Acta Neuropathologica
- Effect of dietary Lorenzo's oil and docosahexaenoic acid treatment for Zellweger syndromeYasuhiro Arai, Yohei Kitamura, Masaharu Hayashi, Kyoichi Oshida, Toshiaki Shimizu, Yuichiro Yamashiro · 2008 · Congenital Anomalies
- Peroxisomal DiseasesHugo W. Moser · 1993 · Springer eBooks
- Broadening the Spectrum of Adulthood X-Linked Adrenoleukodystrophy: A Report of Two Atypical CasesMatteo Foschi, Veria Vacchiano, Patrizia Avoni, Alex Incensi, Stella Battaglia, Vincenzo Angelo Donadio, Elena Panzeri, Maria Teresa Bassi, Rocco Liguori, Giovanni Rizzo · 2019 · Frontiers in Neurology
- Dentato-olivary dysplasia in sibs: an autosomal recessive disorder?Timothy Martland, Brian N Harding, R E Morton, I Young · 1997 · Journal of Medical Genetics
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- The Zellweger syndrome: Book review and bibliography. The cerebro‐hepato‐renal syndrome of Zellweger. L.C.P. Govaerts. Nijmegen: Stichting Studentenpers, 1984, 195 pp.John M. Opitz · 1985 · American Journal of Medical Genetics
- Clinicopathologic conference: A three‐month‐old infant with failure to thrive, hepatomegaly, and neurological impairmentAaron Friedman, James Bethzhold, Richard Hong, Enid F. Gilbert, Chirane Viseskul, John M. Opitz · 1980 · American Journal of Medical Genetics
- Peroxisome Deficiency Impairs BDNF Signaling and MemoryYuichi Abe, Yoshiki Nishimura, Kaori Nakamura, Shigehiko Tamura, Masanori Honsho, Hiroshi Udo, Toshihide Yamashita, Yukio Fujiki · 2020 · Frontiers in Cell and Developmental Biology
- Neuroanatomical study of somatomotor cortex in microcephalic mice induced by cytosine arabinosideMasaki Ohno · 1984 · Brain and Development
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- Polymicrogyrie bifrontale et syndrome d'Ehlers-DanlosH. Ezzeddine, Pascal Sabouraud, Catherine Eschard, O. El Tourjuman, Nathalie Bednarek, J. Motte · 2005 · Archives de Pédiatrie
- Mouse Models for Peroxisome Biogenesis DisordersMyriam I Baes · 2000 · Cell Biochemistry and Biophysics
- Peroxisomal bifunctional enzyme deficiency: serial neurophysiological examinations of a caseShinjiro Akaboshi, Yutaka Tomita, Yasuyuki Suzuki, Mizuho Une, Osamu Sohma, Sachio Takashima, Kenzo Takeshita · 1997 · Brain and Development
- Genetic Metabolic DiseaseDavid R FitzPatrick · 2007 · Springer eBooks
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- Cerebral dysgeneses secondary to metabolic disorders in fetal lifeWilliam David Graf · 2007 · Handbook of clinical neurology
- Rhizomelic chondrodysplasia punctata: 16-year follow-up of a child from birth.Carlo Lenti, P. Paganoni, Roberto Sangermani · 1991 · PubMed
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- Cerebral and Cranial MalformationsClaus Diebler, Olivier Dulac · 1987 · Springer eBooks
- Molecular cloning of Chinese hamster ceramide glucosyltransferase and its enhanced expression in peroxisome-defective mutant Z65 cellsMakiko Saito, Yasushi Fukushima, Ken Tatsumi, Lin Bei, Yukio Fujiki, Masao Iwamori, Takashi Igarashi, Yoichi Sakakihara · 2002 · Archives of Biochemistry and Biophysics
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- Complex glycerol kinase deficiency: A contiguous gene syndrome involving the Duchenne muscular dystrophy, glycerol kinase, and adrenal hypoplasia congenita lociEdward R.B. McCabe, Weiwen Guo, Thomas P. Burris · 1996 · Mental Retardation and Developmental Disabilities Research Reviews
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- A Mouse Model System to Study Peroxisomal Roles in Neurodegeneration of Peroxisome Biogenesis DisordersYuichi Abe, Shigehiko Tamura, Masanori Honsho, Yukio Fujiki · 2020 · Advances in experimental medicine and biology
- The cDNA Sequence and Expression of the AAA-family Peroxin Genespex-1andpex-6from the Nematode Caenorhabditis elegansSimona Ghenea, Masaki Takeuchi, Junko Motoyama, Kumiko Sasamoto, Wolf‐H. Kunau, Tatsuyuki Kamiryo, Masanori Bun‐ya · 2001 · ZOOLOGICAL SCIENCE
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- Peroxisomal DisordersHugo W. Moser · 1999 · Elsevier eBooks
- Zellweger Cerebrohepatorenal SyndromeJacob Valk, Marjo S. van der Knaap · 1989 · Springer eBooks
- PolymicrogyriaJeffrey Alan Golden · 2018 · Wiley eBooks
- Dysregulated lipid metabolism and hypomyelination in postnatal peroxisome-deficient Pex2 knockout Zellweger miceTanja Eberhart, Khanichi N. Charles, Brenda Salumbides-Torres, Nia Price, Steven J. Fliesler, Phyllis L. Faust, Werner J. Kovacs · 2026 · Frontiers in Molecular Neuroscience
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- Degenerative Diseases of the NewbornJoseph J. Volpe · 2008 · Elsevier eBooks
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- Docosahexaenoic Acid Therapy for Disorders of Peroxisome BiogenesisHugo W. Moser, Gerald V. Raymond · 2001 · Humana Press eBooks
- Neurobiology of Peroxisomal DisordersJames M. Powers · 2007 · Elsevier eBooks
- Malformations cérébrales et maladies métaboliquesNathalie Bednarek, H. Ezzédine, Christopher Sommer, Bénédicte Gaillard Leroux, P Morville · 2000 · Archives de Pédiatrie
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- Peroxisomes and Peroxisomal DisordersMarjo S. van der Knaap, Jacob Valk · 1995 · Springer eBooks
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