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A neurodevelopmental approach to the classification of schizophrenia.
Murray RM, O'Callaghan E, Castle DJ, Lewis SW. Murray RM, et al. Schizophr Bull. 1992;18(2):319-32. doi: 10.1093/schbul/18.2.319. Schizophr Bull. 1992. PMID: 1377834 Review.
The conventional distinction between schizophrenia and manic depression has received little objective support from recent studies of phenomenology, outcome, or familial homotypy. Instead, much clinical, epidemiological, and morphological evidence suggests that within the b …
The conventional distinction between schizophrenia and manic depression has received little objective support from recent studies of phenome …
The Species Problem from the Modeler's Point of View.
Manceau M, Lambert A. Manceau M, et al. Bull Math Biol. 2019 Mar;81(3):878-898. doi: 10.1007/s11538-018-00536-2. Epub 2018 Dec 7. Bull Math Biol. 2019. PMID: 30535845
We specify three desirable properties of species partitions: (A) Heterotypy between species, (B) Homotypy within species and (M) Genealogical monophyly of each species. ...
We specify three desirable properties of species partitions: (A) Heterotypy between species, (B) Homotypy within species and (M) Gene …
Many different tumor types have polyclonal tumor origin: evidence and implications.
Parsons BL. Parsons BL. Mutat Res. 2008 Sep-Oct;659(3):232-47. doi: 10.1016/j.mrrev.2008.05.004. Epub 2008 Jul 9. Mutat Res. 2008. PMID: 18614394 Review.
Yet, recent findings regarding X chromosome inactivation patch size indicate that the X-linked marker data previously interpreted as evidence of monoclonal tumor origin is actually more consistent with polyclonal tumor origin, a situation where two or more cells or clones of cell …
Yet, recent findings regarding X chromosome inactivation patch size indicate that the X-linked marker data previously interpreted as evidenc …
Transdiagnostic clinical staging in youth mental health: a first international consensus statement.
Shah JL, Scott J, McGorry PD, Cross SPM, Keshavan MS, Nelson B, Wood SJ, Marwaha S, Yung AR, Scott EM, Öngür D, Conus P, Henry C, Hickie IB; International Working Group on Transdiagnostic Clinical Staging in Youth Mental Health. Shah JL, et al. World Psychiatry. 2020 Jun;19(2):233-242. doi: 10.1002/wps.20745. World Psychiatry. 2020. PMID: 32394576 Free PMC article.
Progressive pontobulbar palsy with deafness: clinical and pathological study of two cases.
Brucher JM, Dom R, Lombaert A, Carton H. Brucher JM, et al. Arch Neurol. 1981 Mar;38(3):186-90. doi: 10.1001/archneur.1981.00510030080012. Arch Neurol. 1981. PMID: 6970563
There are differences from other forms of bulbar paralysis, lower motor neuron diseases, and some spinocerebellar hereditary affections. In view of the homochrony and homotypy in familial cases and the pathological findings, progressive pontobulbar palsy with deafness appe …
There are differences from other forms of bulbar paralysis, lower motor neuron diseases, and some spinocerebellar hereditary affections. In …
The organization of neocortical projections from the ventroposterior thalamic complex in the marsupial brush-tailed possum, Trichosurus vulpecula: a horseradish peroxidase study.
Haight JR, Neylon L. Haight JR, et al. J Anat. 1978 Aug;126(Pt 3):459-85. J Anat. 1978. PMID: 689987 Free PMC article.
The dorsomedial division of VP or VPM projects uniformly to cortex from all areas of that subnucleus, but the strict homotypy characteristic of VPL's projection was not as apparent. VPM also projects to two distinct regions within its cortical field. ...
The dorsomedial division of VP or VPM projects uniformly to cortex from all areas of that subnucleus, but the strict homotypy charact …
The protracted form of juvenile neuronal ceroid-lipofuscinosis.
Goebel HH, Pilz H, Gullotta F. Goebel HH, et al. Acta Neuropathol. 1976 Dec 21;36(4):393-6. doi: 10.1007/BF00699645. Acta Neuropathol. 1976. PMID: 189559
Clinical and ultrastructural findings consisting of curvilinear and fingerprint residual bodies, in a protracted juvenile form of NCL are reported from a woman who died at the age of 35 years. Homochrony and homotypy of her brother's illness emphasize intrafamilial similar …
Clinical and ultrastructural findings consisting of curvilinear and fingerprint residual bodies, in a protracted juvenile form of NCL are re …
Adult ceroid-lipofuscinosis (Kufs' disease) in two brothers. Retinal and visceral storage in one; diagnostic muscle biopsy in the other.
Dom R, Brucher JM, Ceuterick C, Carton H, Martin JJ. Dom R, et al. Acta Neuropathol. 1979 Jan 12;45(1):67-72. doi: 10.1007/BF00691807. Acta Neuropathol. 1979. PMID: 760366
Two brothers developed a neurological condition characterized by homochrony and homotypy: the first symptoms in both were generalized epileptic seizures, occurring at about the same age (30 years in the elder, 32 years in the younger), followed by a cerebellar syndrome wit …
Two brothers developed a neurological condition characterized by homochrony and homotypy: the first symptoms in both were generalized …