| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| J E Pittella, A M Nogueir. [Cerebellar agenesia associated with microencephaly and agyria: report of an autopsied case in a newborn infant and a review of the literature]. Arquivos de neuro-psiquiatria. vol 46. issue 4. 1989-06-02. PMID:3072938. |
a post-mortem examined case of cerebellar agenesis associated with microcephaly, agyria and deformities of the extremities and of the external ear in a newborn is presented. |
1989-06-02 |
2023-08-11 |
Not clear |
| G S Pai, S Morgan, C Whetsel. Etiologic heterogeneity in dyskeratosis congenita. American journal of medical genetics. vol 32. issue 1. 1989-05-19. PMID:2705484. |
severe microcephaly, mental retardation, cerebellar hypoplasia, and purple discoloration of the tongue were other manifestations not usually seen in dc. |
1989-05-19 |
2023-08-11 |
Not clear |
| S Hreidarsson, K Kristjansson, G Johannesson, J H Johannsso. A syndrome of progressive pancytopenia with microcephaly, cerebellar hypoplasia and growth failure. Acta paediatrica Scandinavica. vol 77. issue 5. 1989-01-23. PMID:3201986. |
a syndrome of progressive pancytopenia with microcephaly, cerebellar hypoplasia and growth failure. |
1989-01-23 |
2023-08-11 |
Not clear |
| S Hreidarsson, K Kristjansson, G Johannesson, J H Johannsso. A syndrome of progressive pancytopenia with microcephaly, cerebellar hypoplasia and growth failure. Acta paediatrica Scandinavica. vol 77. issue 5. 1989-01-23. PMID:3201986. |
other findings included microcephaly with cerebellar hypoplasia, growth failure of prenatal onset and severe psychomotor retardation. |
1989-01-23 |
2023-08-11 |
Not clear |
| T I Ostrovskaya, G I Lazju. Cerebral abnormalities in the Neu-Laxova syndrome. American journal of medical genetics. vol 30. issue 3. 1988-12-07. PMID:3055985. |
cerebral abnormalities are considered an obligatory manifestation of the neu-laxova syndrome and include lissencephaly, severe microcephaly, aplasia of the corpus callosum, hypoplasia of the cerebellum, and other pathological changes. |
1988-12-07 |
2023-08-11 |
human |
| H Nishio, S Kodama, T Matsuo, M Ichihashi, H Ito, Y Fujiwar. Cockayne syndrome: magnetic resonance images of the brain in a severe form with early onset. Journal of inherited metabolic disease. vol 11. issue 1. 1988-05-13. PMID:3128691. |
autopsy revealed severe microcephaly, severe atrophy of cerebrum, cerebellum and brain stem, and calcification throughout the brain, especially in the basal ganglia. |
1988-05-13 |
2023-08-11 |
Not clear |
| b' I Ferrer, E Galofr\\xc3\\xa. Dendritic spine anomalies in fetal alcohol syndrome. Neuropediatrics. vol 18. issue 3. 1987-12-22. PMID:3683757.' |
neuropathological findings in the brain of a 4-month-old child born to a chronic alcoholic mother were microcephaly, uncovered rostral region of the insula, disordered arrangement of nerve cells in the cerebral cortex, cerebellar abnormalities, and glial meningeal heterotopies. |
1987-12-22 |
2023-08-11 |
Not clear |
| O Robain, O Dulac, J Lejeun. Cerebellar hemispheric agenesis. Acta neuropathologica. vol 74. issue 2. 1987-12-07. PMID:3673512. |
the relation of cerebellar agenesis with basal ganglia abnormalities and microcephaly is discussed. |
1987-12-07 |
2023-08-11 |
Not clear |
| Y Nakamura, H Nakashima, S Fukuda, T Hashimoto, M Maruyam. Bilateral cystic nephroblastomas and multiple malformations with trisomy 8 mosaicism. Human pathology. vol 16. issue 7. 1985-08-15. PMID:2989151. |
the case of a 16-month-old female infant with bilateral cystic nephroblastomas, dandy-walker syndrome, microcephaly, bilateral cataracts, and cerebellar heterotopia is reported. |
1985-08-15 |
2023-08-11 |
Not clear |
| D Soffer, H W Grotsky, I Rapin, K Suzuk. Cockayne syndrome: unusual neuropathological findings and review of the literature. Annals of neurology. vol 6. issue 4. 1981-03-17. PMID:400082. |
these included microcephaly, white matter atrophy with patchy loss of myelinated fibers, calcifications of the basal ganglia, occasional ferrugination of cerebral and cerebellar neurons, and severe cerebellar degeneration. |
1981-03-17 |
2023-08-11 |
human |
| V A Aleksandrov, D Schreibe. [Combined transplacental carcinogenic action of N-nitrosomethylurea (NMU) and N-nitrosoethylurea (NEU) in rats]. Voprosy onkologii. vol 24. issue 4. 1978-07-24. PMID:654172. |
to induce brain defects such as microcephaly nmu was injected on the 15th day, whereas to induce cerebellar defects- on the 21st day of embryogenesis. |
1978-07-24 |
2023-08-11 |
rat |
| R R Heffne. Syndrome of absent abdominal muscles: two cases with microcephaly, polymicrogyria, and cerebellar malformations. Journal of neurology, neurosurgery, and psychiatry. vol 33. issue 6. 1971-03-23. PMID:4250700. |
syndrome of absent abdominal muscles: two cases with microcephaly, polymicrogyria, and cerebellar malformations. |
1971-03-23 |
2023-08-11 |
Not clear |
| R R Heffne. Syndrome of absent abdominal muscles: two cases with microcephaly, polymicrogyria, and cerebellar malformations. Journal of neurology, neurosurgery, and psychiatry. vol 33. issue 6. 1971-03-23. PMID:4250700. |
microcephaly, polymicrogyria, and cerebellar heterotopiae were present in both. |
1971-03-23 |
2023-08-11 |
Not clear |