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humans (6) 6
index medicus (5) 5
adult (4) 4
female (4) 4
male (4) 4
genetics & heredity (3) 3
adenosine triphosphatases - genetics (2) 2
article (2) 2
autosomal dominant (2) 2
cell cycle proteins - genetics (2) 2
diagnosis (2) 2
family (2) 2
frontotemporal dementia (2) 2
middle aged (2) 2
muscle, skeletal - pathology (2) 2
osteitis deformans - complications (2) 2
pedigree (2) 2
retrospective studies (2) 2
surgery (2) 2
valosin containing protein (2) 2
valosin-containing-protein (2) 2
abridged index medicus (1) 1
adenosine triphosphatases - metabolism (1) 1
adept (1) 1
adhesions (1) 1
adipose tissue (1) 1
age of onset (1) 1
aged (1) 1
alzheimer-disease (1) 1
amyotrophic lateral sclerosis (1) 1
analysis (1) 1
atpase (1) 1
barrier system (1) 1
biopsy (1) 1
blood transfusion (1) 1
body composition (1) 1
bone diseases (1) 1
cell cycle proteins - metabolism (1) 1
chromosome 9p13.3-12 (1) 1
chromosome 9p13.3‐12 (1) 1
chromosomes, human, pair 4 - genetics (1) 1
coagulopathy (1) 1
colorectal surgery (1) 1
complications (1) 1
criteria (1) 1
cross-sectional studies (1) 1
dementia (1) 1
dementia - complications (1) 1
dementia - genetics (1) 1
disorder (1) 1
electromyography (1) 1
essential tremor - genetics (1) 1
exons (1) 1
familial essential tremor (1) 1
family health (1) 1
frontotemporal dementia - complications (1) 1
frontotemporal dementia - diagnosis (1) 1
frontotemporal dementia - mortality (1) 1
gastrointestinal diseases (1) 1
gene (1) 1
gene-mutations (1) 1
general surgery - education (1) 1
genes (1) 1
genes, dominant - genetics (1) 1
genetic aspects (1) 1
genetic association studies (1) 1
genetic linkage (1) 1
genetic variation (1) 1
genomics (1) 1
genotype (1) 1
genotype & phenotype (1) 1
genotype-phenotype (1) 1
genotype–phenotype (1) 1
growth (1) 1
growth-factor (1) 1
hemorrhage - mortality (1) 1
hemorrhage - surgery (1) 1
hereditary inclusion body myopathy (1) 1
heterogeneity (1) 1
hyalobarrier (1) 1
hyaluronic acid (1) 1
inclusion bodies - ultrastructure (1) 1
inclusion body myopathy (1) 1
inclusion-body myositis (1) 1
infant (1) 1
informed consent (1) 1
informed-consent (1) 1
injury severity score (1) 1
interceed (1) 1
intercoat (1) 1
internship and residency (1) 1
intestinal-obstruction (1) 1
intraperitoneal adhesions (1) 1
kidney transplantation - education (1) 1
kidney transplantation - methods (1) 1
laparotomy - methods (1) 1
laparotomy - mortality (1) 1
limb-girdle muscular dystrophy (1) 1
limb‐girdle muscular dystrophy (1) 1
linkage analysis (1) 1
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1. Full Text The Strength of Generations
by Kimonis, Katerina O., MD, MPH and Rajab, Taufiek Konrad, MD, BChir
American Journal of Kidney Diseases, ISSN 0272-6386, 2013, Volume 61, Issue 5, pp. A22 - A23
Nephrology | UROLOGY & NEPHROLOGY
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2. Full Text Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia
by Kimonis, Virginia. E and Mehta, Sarju G and Fulchiero, Erin C and Thomasova, Dana and Pasquali, Marzia and Boycott, Kym and Neilan, Edward G and Kartashov, Alex and Forman, Mark S and Tucker, Stuart and Kimonis, Katerina and Mumm, Steven and Whyte, Michael P and Smith, Charles D and Watts, Giles D. J
American Journal of Medical Genetics Part A, ISSN 1552-4825, 03/2008, Volume 146A, Issue 6, pp. 745 - 757
Inclusion body myopathy with Paget disease of the bone (PDB) and/or frontotemporal dementia (IBMPFD, OMIM 167320), is a progressive autosomal dominant disorder... 
Paget disease of bone | chromosome 9p13.3‐12 | frontotemporal dementia | autosomal dominant | hereditary inclusion body myopathy | limb‐girdle muscular dystrophy | VCP (valosin‐containing protein) | Autosomal dominant | Limb-girdle muscular dystrophy | VCP (valosin-containing protein) | Hereditary inclusion body myopathy | Frontotemporal dementia | Chromosome 9p13.3-12 | GENE-MUTATIONS | ALZHEIMER-DISEASE | DIAGNOSIS | VALOSIN-CONTAINING-PROTEIN | ATPASE | chromosome 9p13.3-12 | INCLUSION-BODY MYOSITIS | limb-girdle muscular dystrophy | P97 | PATHOGENESIS | PROTEASOME | GENETICS & HEREDITY | DISORDER | Inclusion Bodies - ultrastructure | Cross-Sectional Studies | Humans | Middle Aged | Valosin Containing Protein | Muscle, Skeletal - ultrastructure | Male | Dementia - genetics | Osteitis Deformans - genetics | Osteitis Deformans - complications | Dementia - complications | Pedigree | Cell Cycle Proteins - genetics | Muscular Diseases - complications | Adult | Family | Female | Adenosine Triphosphatases - genetics | Retrospective Studies | Muscle, Skeletal - pathology | Muscular Diseases - genetics
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3. Full Text The strength of generations
by Kimonis, Katerina O and Rajab, Taufiek Konrad
American journal of kidney diseases : the official journal of the National Kidney Foundation, 05/2013, Volume 61, Issue 5, p. xxii
Internship and Residency | Kidney Transplantation - education | Humans | General Surgery - education | Kidney Transplantation - methods | Polycystic Kidney, Autosomal Dominant - surgery
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4. Full Text Practical implications of postoperative adhesions for preoperative consent and operative technique
by Rajab, Taufiek Konrad and Kimonis, Katerina O and Ali, Erden and Offodile, Anaeze C and Brady, Matthew and Bleday, Ronald
International Journal of Surgery, ISSN 1743-9191, 2013, Volume 11, Issue 9, pp. 753 - 756
Abstract Adhesions complicate most intra-peritoneal operations. Once adhesions have formed, patients are at life-long risk for complications that include small... 
Surgery | Spraygel | Adhesions | Adept | Informed consent | Interceed | Hyalobarrier | Intercoat | Seprafilm | COLORECTAL SURGERY | SURGERY | INTRAPERITONEAL ADHESIONS | RANDOMIZED CLINICAL-TRIAL | SMALL-BOWEL OBSTRUCTION | BARRIER SYSTEM | INFORMED-CONSENT | COMPLICATIONS | GROWTH-FACTOR | INTESTINAL-OBSTRUCTION | POUCH-ANAL ANASTOMOSIS | Informed Consent | Peritoneal Cavity - surgery | Hyaluronic Acid | Tissue Adhesions | Humans | Preoperative Care | Surgeons | Gastrointestinal diseases | Methods
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5. Full Text Genetic heterogeneity in autosomal dominant essential tremor
by Kovach, Margaret J and Ruiz, Jimmy and Kimonis, Katerina and Mueed, Sajjad and Sinha, Shobhit and Higgins, Connie and Elble, Suzanne and Elble, Rodger and Kimonis, Virginia E
Genetics in Medicine, ISSN 1098-3600, 2001, Volume 3, Issue 3, pp. 197 - 199
Purpose: To perform linkage analysis of candidate loci in a large Midwestern family with autosomal dominant essential tremor. Methods: Thirty-eight members of... 
Autosomal dominant | Familial essential tremor | Linkage analysis | CRITERIA | DIAGNOSIS | familial essential tremor | linkage analysis | MAPS | GENETICS & HEREDITY | autosomal dominant | Essential Tremor - genetics | Humans | Family Health | Male | Chromosomes, Human, Pair 4 - genetics | Lod Score | Genetic Variation | Phenotype | Pedigree | Age of Onset | Adult | Female | Genes, Dominant - genetics | Microsatellite Repeats | Genetic Linkage
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6. Full Text Damage Control Resuscitation in Combination With Damage Control Laparotomy: A Survival Advantage
by Duchesne, Juan C and Kimonis, Katerina and Marr, Alan B and Rennie, Kelly V and Wahl, Georgia and Wells, Joel E and Islam, Tareq M and Meade, Peter and Stuke, Lance and Barbeau, James M and Hunt, John P and Baker, Christopher C and McSwain, Norman E
The Journal of Trauma: Injury, Infection, and Critical Care, ISSN 0022-5282, 07/2010, Volume 69, Issue 1, pp. 46 - 52
BACKGROUND:Damage control laparotomy (DCL) improves outcomes when used in patients with severe hemorrhage. Correction of coagulopathy with close ratio... 
Obesity | Infant | Adipose tissue | Newborn | Growth | Body composition | MORTALITY | SURGERY | RATIO | MASSIVE TRANSFUSION | COAGULOPATHY | PENETRATING ABDOMINAL INJURY | STRATEGIES | PLASMA | PATIENT | TRAUMA | Multivariate Analysis | Wounds, Nonpenetrating - surgery | Wounds and Injuries - surgery | Resuscitation - methods | Humans | Hemorrhage - mortality | Male | Wounds, Penetrating - mortality | Wounds, Penetrating - surgery | Injury Severity Score | Laparotomy - mortality | Wounds and Injuries - mortality | Regression Analysis | Blood Transfusion | Laparotomy - methods | Wounds, Nonpenetrating - mortality | Survival Analysis | Adult | Female | Retrospective Studies | Hemorrhage - surgery | Rehydration Solutions - therapeutic use | Resuscitation - mortality
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7. Full Text Genotype–phenotype studies of VCP‐associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia
by Mehta, SG and Khare, M and Ramani, R and Watts, GDJ and Simon, M and Osann, KE and Donkervoort, S and Dec, E and Nalbandian, A and Platt, J and Pasquali, M and Wang, A and Mozaffar, T and Smith, CD and Kimonis, VE
Clinical Genetics, ISSN 0009-9163, 05/2013, Volume 83, Issue 5, pp. 422 - 431
Valosin containing protein (VCP) disease associated with inclusion body myopathy, Paget disease of the bone and frontotemporal dementia is a progressive... 
genotype–phenotype | valosin containing protein | frontotemporal dementia | amyotrophic lateral sclerosis | inclusion body myopathy | Paget's disease of bone | Amyotrophic lateral sclerosis | Inclusion body myopathy | Valosin containing protein | Frontotemporal dementia | Genotype-phenotype | VALOSIN-CONTAINING-PROTEIN | LOBAR DEGENERATION | genotype-phenotype | FAMILY | HETEROGENEITY | GENE | TDP-43 | MUTATION | GENETICS & HEREDITY | Exons | Humans | Middle Aged | Valosin Containing Protein | Male | Frontotemporal Dementia - mortality | Osteitis Deformans - diagnosis | Young Adult | Frontotemporal Dementia - complications | Myositis, Inclusion Body - diagnosis | Myositis, Inclusion Body - mortality | Cell Cycle Proteins - genetics | Adult | Female | Electromyography | Genetic Association Studies | Osteitis Deformans - mortality | Cell Cycle Proteins - metabolism | Adenosine Triphosphatases - metabolism | Genotype | Neural Conduction | Frontotemporal Dementia - diagnosis | Myositis, Inclusion Body - genetics | Osteitis Deformans - complications | Biopsy | Myositis, Inclusion Body - complications | Adenosine Triphosphatases - genetics | Aged | Muscle, Skeletal - pathology | Mutation | Medical research | Analysis | Genes | Medical genetics | Medicine, Experimental | Genetic aspects | Dementia | Proteins | Genotype & phenotype | Pathology | Bone diseases | Genomics | Paget’s disease of bone
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