A Golgi study of the brain malformation in Zellweger's cerebro-hepato-renal disease

scientific article published on 01 January 1981

A Golgi study of the brain malformation in Zellweger's cerebro-hepato-renal disease is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1007/BF00691526
P698PubMed publication ID7348002

P2093author name stringA M Goffinet
P Landrieu
G Lyon
E Della Giustina
P2860cites workCerebro-hepato-renal syndrome of Zellweger. A report of eight cases with comments upon the incidence, the liver lesion, and a fault in pipecolic acid metabolismQ28337179
A FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTSQ34257272
Weaver Mutant Mouse Cerebellum: Defective Neuronal Migration Secondary to Abnormality of Bergmann GliaQ35094240
Anatomical, Physiological and biochemical studies of the cerebellum fromreelermutant mouseQ39177078
Mechanisms of Cortical Development: A View From Mutations in MiceQ39811367
The mechanism of arrest of neuronal migration in the Zellweger malformation: An hypothesis based upon cytoarchitectonic analysisQ41038903
Neuropathological considerations in cerebro-hepato-renal syndrome (Zellweger's syndrome)Q48397268
Anatomical, physiological and biochemical studies of the cerebellum from mutant mice. II. Morphological study of cerebellar cortical neurons and circuits in the weaver mouseQ48445395
The Neuropathology of a Peculiar Form of Cerebro-Renal Syndrome in a ChildQ48644244
Cerebro-hepato-renal syndrome of Zellweger. Two patients with islet cell hyperplasia, hypoglycemia, and thymic anomalies, and comments on iron metabolismQ48712587
Cerebro-hepato-renal syndrome. Report of a caseQ48986762
Cerebro-hepato-renal syndrome of Zellweger: an inherited disorder of neuronal migrationQ50644403
Cerebro-hepato-renal syndrome. A newly recognized hereditary disorder of multiple congenital defects, including sudanophilic leukodystrophy, cirrhosis of the liver, and polycystic kidneysQ51203911
An autoradiographic analysis of histogenesis in the mouse cerebellumQ51299748
A syndrome of multiple developmental defects including polycystic kidneys and intrahepatic biliary dysgenesis in 2 siblings.Q52348415
Cerebro-hepato-renal Syndrome of ZellwegerQ54717391
[Normal development and dysgenesias of the dentate nucleus and inferior olive (author's transl)]Q68776347
Oculocerebral malformations. A reappraisal of Walker's 'lissencephaly'Q71494148
P433issue1
P304page(s)23-28
P577publication date1981-01-01
P1433published inActa NeuropathologicaQ343168
P1476titleA Golgi study of the brain malformation in Zellweger's cerebro-hepato-renal disease
P478volume55

Reverse relations

cites work (P2860)
Q48261562A Golgi study of the cerebral cortex in Fukuyama-type congenital muscular dystrophy, Walker-type "lissencephaly," and classical lissencephaly.
Q38493264Cerebellar alterations induced by chronic hypoxia: an immunohistochemical study using a chick embryonic model
Q44573718Cerebral abnormalities in thanatophoric dysplasia
Q42468439Cortical Dysgenesis in a Variant of Phenylketonuria (Dihydropteridine Reductase Deficiency)
Q48735085Cortical cytoarchitectural and immunohistochemical studies on Zellweger syndrome
Q41253593Cortical dysplasia in Fukuyama congenital muscular dystrophy (FCMD): a Golgi and angioarchitectonic analysis
Q39757600Disorders of neuronal migration
Q70636706Fine structure based on the Golgi method of the abnormal cortex and heterotopic nodules in pachygyria
Q41790709Nephrosis and disturbances of neuronal migration in male siblings--a new hereditary disorder?
Q41934714Neuroanatomical study of somatomotor cortex in microcephalic mice induced by cytosine arabinoside
Q48573354Neuropathological and Golgi study on a case of thanatophotoric dysplasia
Q38145146Organelle pathology in metabolic neuromuscular disease: an overview
Q68551112Peroxisomal beta-oxidation defect with detectable peroxisomes: a case with neonatal onset and progressive course
Q53771743Progressive neurologic deterioration in a hypotonic infant.
Q40655527The place of neuronal migration abnormalities in child neurology.
Q36684338Wiring, dysmorphogenesis and epilepsy: A hypothesis

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