P C Patsalis
Overview
Explore the profile of P C Patsalis including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
32
Citations
422
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Aweimer A, El-Battrawy I, Akin I, Borggrefe M, Mugge A, Patsalis P, et al.
J Intern Med
. 2020 Nov;
289(5):675-687.
PMID: 33179374
Background: Several reports have described Takotsubo syndrome (TTS) secondary to thyrotoxicosis. A complex interaction of central and peripheral catecholamines with thyroid homeostasis has been suggested. In this study, we analysed...
2.
Basehore M, Michaelson-Cohen R, Levy-Lahad E, Sismani C, Bird L, Friez M, et al.
Clin Genet
. 2014 May;
87(5):461-6.
PMID: 24805811
Alpha-thalassemia intellectual disability, one of the recognizable X-linked disability syndromes, is characterized by short stature, microcephaly, distinctive facies, hypotonic appearance, cardiac and genital anomalies, and marked skewing of X-inactivation in...
3.
Sismani C, Donoghue J, Alexandrou A, Karkaletsi M, Christopoulou S, Konstantinidou A, et al.
Gene
. 2013 Aug;
530(1):138-42.
PMID: 23973723
Duplications of the X chromosome are rare cytogenetic findings, and have been associated with an abnormal phenotype in the male offspring of apparently normal or near normal female carriers. We...
4.
Dixit A, McKee S, Mansour S, Mehta S, Tanteles G, Anastasiadou V, et al.
Clin Genet
. 2012 Feb;
83(2):155-61.
PMID: 22369319
Williams-Beuren syndrome is a well-known microdeletion syndrome with a recognizable clinical phenotype. The subtle phenotype of the reciprocal microduplication of the Williams-Beuren critical region has been described recently. We report...
5.
Liehr T, Stumm M, Wegner R, Bhatt S, Hickmann P, Patsalis P, et al.
Cytogenet Genome Res
. 2009 Apr;
124(1):102-5.
PMID: 19372675
Directly transmitted unbalanced chromosomal abnormalities (UBCA) or euchromatic variants (EV) were recently reported for >50 euchromatic regions of almost all human autosomes. UBCA and EV are comprised of a few...
6.
Kitsiou-Tzeli S, Sismani C, Karkaletsi M, Florentin L, Anastassiou A, Koumbaris G, et al.
Prenat Diagn
. 2008 Jul;
28(8):770-2.
PMID: 18615545
No abstract available.
7.
Velissariou V, Sismani C, Christopoulou S, Kaminopetros P, Hatzaki A, Evangelidou P, et al.
Eur J Med Genet
. 2007 Jun;
50(4):291-300.
PMID: 17584536
Two cases of rare structural aberrations of the Y chromosome were detected: a del(Y) (q12) chromosome in a child with mild dysmorphic features, obesity and psychomotor delay, and two identical...
8.
Patsalis P
Genet Couns
. 2007 May;
18(1):57-69.
PMID: 17515301
Complex Chromosomal Rearrangements (CCRs) are constitutional structural rearrangements involving three or more chromosomes or having more than two breakpoints. CCRs preferentially occur during spermatogenesis and are transmitted in families through...
9.
Ioulianos A, Sismani C, Fourouclas N, Patroclou T, Sergiou C, Patsalis P
Int J Androl
. 2002 May;
25(3):153-8.
PMID: 12031043
Y chromosome microdeletions in the azoospermia factor (AZF) locus have been associated with spermatogenic failure. The frequency of AZF deletions is estimated to be about 10-18% in subgroups of idiopathic...
10.
Sismani C, Armour J, Flint J, Girgalli C, Regan R, Patsalis P
Eur J Hum Genet
. 2001 Jul;
9(7):527-32.
PMID: 11464244
Subtelomeric chromosomal abnormalities are emerging as an important cause of human genetic disorders. The scope of this investigation was to screen a selected group of children with idiopathic mental retardation...