Classification of Endogenous Psychoses and Their Differentiated Etiology 1999
DOI: 10.1007/978-3-7091-6371-9_9
|View full text |Cite
|
Sign up to set email alerts
|

Etiology of Endogenous Psychoses

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

4
43
0
1

Year Published

2002
2002
2024
2024

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 27 publications
(48 citation statements)
references
References 0 publications
4
43
0
1
Order By: Relevance
“…We found an overlap with Leonhard's system of schizophrenias [10] . He described cycloid and unsystematic schizophrenias as having a periodic and bipolar course pattern in most cases, while systematic schizophrenias show a progressive symptomatology.…”
Section: Impact Of a System-specific Typologymentioning
confidence: 67%
See 3 more Smart Citations
“…We found an overlap with Leonhard's system of schizophrenias [10] . He described cycloid and unsystematic schizophrenias as having a periodic and bipolar course pattern in most cases, while systematic schizophrenias show a progressive symptomatology.…”
Section: Impact Of a System-specific Typologymentioning
confidence: 67%
“…According to the concept of Huber [7,8,9] , 20 patients were in full remission, 27 showed uncharacteristic residues, and 53 showed characteristic residues. Finally, according to Leonhard's classification [10] , 52 of the cases were unsystematic schizophrenias, 28 systematic schizophrenias, and 20 cycloid psychoses ( tables 2 , 3 ).…”
Section: Association With Traditional Course Typologiesmentioning
confidence: 99%
See 2 more Smart Citations
“…[11][12][13] In an attempt to reduce genetic heterogeneity, Stober and coworkers restricted a genome wide linkage study to detect schizophrenia susceptibility loci to 12 German families ascertained through a proband who met criteria for periodic catatonia as defined by Leonhard. 11,14 Evidence for linkage was obtained in these pedigrees (average 4.8 affected individuals per pedigree) for chromosome 15q15 at D15S1012 (nonparametric LOD score (NPL) = 3.57, P = 2.6 × 10 −5 ) and chromosome 22q13 at D22S1169 (NPL = 1.85; P = 1.8 × 10 −3 ). The majority of the evidence for linkage to the 22q13 region came from one extended large pedigree with seven affected subjects.…”
mentioning
confidence: 88%