Articles

UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1271) 1271
Book Chapter (24) 24
Newsletter (8) 8
Newspaper Article (7) 7
Magazine Article (3) 3
Dissertation (1) 1
Journal / eJournal (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (1041) 1041
science & technology (916) 916
female (903) 903
life sciences & biomedicine (899) 899
pregnancy (754) 754
hydrops fetalis (499) 499
biological and medical sciences (447) 447
adult (441) 441
medical sciences (440) 440
infant, newborn (385) 385
male (371) 371
obstetrics & gynecology (371) 371
hydrops fetalis - genetics (321) 321
genetics & heredity (302) 302
gynecology. andrology. obstetrics (297) 297
prenatal diagnosis (295) 295
hydrops fetalis - diagnosis (265) 265
pregnancy. fetus. placenta (241) 241
hydrops fetalis - etiology (230) 230
ultrasonography, prenatal (230) 230
hydrops fetalis - diagnostic imaging (186) 186
pediatrics (186) 186
edema (178) 178
gestational age (161) 161
diseases of mother, fetus and pregnancy (146) 146
mutation (131) 131
genetic disorders (121) 121
hematology (117) 117
pregnant women (112) 112
fatal outcome (109) 109
abridged index medicus (103) 103
fetuses (103) 103
management. prenatal diagnosis (101) 101
alpha-thalassemia - genetics (92) 92
retrospective studies (91) 91
hydrops fetalis - pathology (89) 89
fetal diseases - diagnosis (88) 88
hydrops (87) 87
dropsy (82) 82
infant (78) 78
prenatal diagnosis - methods (76) 76
ultrasonography (76) 76
fetal hydrops (75) 75
medical genetics (75) 75
diagnosis (74) 74
health aspects (70) 70
polymerase chain reaction (70) 70
prognosis (69) 69
analysis (68) 68
hemoglobins, abnormal - genetics (68) 68
pregnancy outcome (68) 68
karyotyping (67) 67
diagnosis, differential (66) 66
fetal death (66) 66
fetus (66) 66
genetic aspects (66) 66
syndrome (66) 66
hydrops fetalis - therapy (64) 64
adolescent (63) 63
research (63) 63
pathology (61) 61
anemia (59) 59
ultrasound (59) 59
pedigree (58) 58
hydrops fetalis - complications (57) 57
infants (57) 57
phenotype (57) 57
animals (56) 56
homozygote (56) 56
risk factors (56) 56
alpha-thalassemia - diagnosis (55) 55
pregnancy trimester, second (52) 52
amniocentesis (51) 51
anemia, hemolytic, congenital - genetics (51) 51
chromosome aberrations (51) 51
child, preschool (50) 50
fetal diseases - genetics (50) 50
hydrops fetalis - blood (49) 49
abnormalities, multiple - genetics (48) 48
fundamental and applied biological sciences. psychology (47) 47
hematologic and hematopoietic diseases (47) 47
thalassemia (47) 47
care and treatment (46) 46
fetal diseases - diagnostic imaging (46) 46
hydrops fetalis - epidemiology (46) 46
hydrops fetalis - virology (46) 46
medicine & public health (46) 46
technology (46) 46
treatment outcome (45) 45
child (44) 44
heterozygote (44) 44
radiology, nuclear medicine & medical imaging (44) 44
hydrops fetalis - mortality (43) 43
acoustics (42) 42
genotype (42) 42
delivery. postpartum. lactation (41) 41
base sequence (40) 40
hemoglobin (40) 40
young adult (40) 40
anemias. hemoglobinopathies (39) 39
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1277) 1277
German (12) 12
French (11) 11
Portuguese (10) 10
Japanese (4) 4
Chinese (3) 3
Hungarian (3) 3
Italian (2) 2
Korean (2) 2
Spanish (2) 2
Danish (1) 1
Dutch (1) 1
Polish (1) 1
Russian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis
by Martin-Almedina, S and Martinez-Corral, I and Holdhus, R and Vicente, A and Fotiou, E and Lin, S and Petersen, K and Simpson, M.A and Hoischen, A and Gilissen, C.F and Jeffery, H and Atton, G and Karapouliou, C and Brice, G and Gordon, K and Wiseman, J.W and Wedin, M and Rockson, S.G and Jeffery, S and Mortimer, P.S and Snyder, M.P and Berland, S and Mansour, S and Makinen, T and Ostergaard, P
The Journal of clinical investigation, ISSN 0021-9738, 2016, Volume 126, Issue 8, pp. 3080 - 3088
Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Endothelial Cells - metabolism | Humans | Mice, Inbred C57BL | Male | Mutation, Missense | Hydrops Fetalis - metabolism | Receptor, EphB4 - metabolism | Exome | Receptor, EphB4 - genetics | Animals | Hydrops Fetalis - genetics | Genes, Dominant | Gene Deletion | Lymphatic Vessels - pathology | HEK293 Cells | Female | Heterozygote | Mice | Mice, Inbred BALB C | Polymorphism, Single Nucleotide | Mutation | Development and progression | Genetic aspects | Gene mutations | Hydrops fetalis | Health aspects | Medical research | Ethics | Edema | Lymphatic system | Biomedical research | Lymphedema | Kinases | Laboratory animals | Index Medicus | Abridged Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis
by Fotiou, Elisavet and Martin-Almedina, Silvia and Simpson, Michael A and Lin, Shin and Gordon, Kristiana and Brice, Glen and Atton, Giles and Jeffery, Iona and Rees, David C and Mignot, Cyril and Vogt, Julie and Homfray, Tessa and Snyder, Michael P and Rockson, Stanley G and Jeffery, Steve and Mortimer, Peter S and Mansour, Sahar and Ostergaard, Pia
Nature communications, ISSN 2041-1723, 09/2015, Volume 6, Issue 1, pp. 8085 - 8085
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Lymphedema - diagnostic imaging | Humans | Lymphangiectasis, Intestinal - genetics | Child, Preschool | Ion Channels - genetics | Male | Lymphangiectasis, Intestinal - diagnostic imaging | Sequence Analysis, DNA | Anemia, Hemolytic, Congenital - genetics | Blotting, Western | Craniofacial Abnormalities - diagnostic imaging | Lymphedema - genetics | Hydrops Fetalis - genetics | Adolescent | Adult | Female | Heterozygote | Mutation | Lymphoscintigraphy | Child | Craniofacial Abnormalities - genetics | Infant, Newborn | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Etiology of non-immune hydrops fetalis: An update
by Bellini, Carlo and Donarini, Gloria and Paladini, Dario and Calevo, Maria Grazia and Bellini, Tommaso and Ramenghi, Luca A and Hennekam, Raoul C
American journal of medical genetics. Part A, ISSN 1552-4825, 2015, Volume 167, Issue 5, pp. 1082 - 1088
hydrops fetalis | classification | systematic review | nonimmune hydrops fetalis | pathophysiology | etiology | Systematic review | Pathophysiology | Etiology | Hydrops fetalis | Classification | Nonimmune hydrops fetalis | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Pregnancy | Humans | Female | Male | Hydrops Fetalis - classification | Hydrops Fetalis - physiopathology | Hydrops Fetalis - etiology | Dropsy | Edema | Development and progression | Analysis | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Electrophoresis features and genotypes of Hb bart's hydrops fetalis
by Li, Youqiong and Liang, Liang and Tian, Mao and Qing, Ting and Wu, Xin
Scandinavian journal of clinical and laboratory investigation, ISSN 0036-5513, 02/2020, Volume 80, Issue 2, pp. 129 - 132
Hb Bart's disease | capillary electrophoresis (CE) | thalassemia | Hydrops fetalis syndrome | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Humans | Hydrops Fetalis - diagnostic imaging | Genotype | Gestational Age | Hemoglobins, Abnormal - analysis | Pregnancy | Hydrops Fetalis - genetics | Ultrasonography, Prenatal | Adult | Female | Mutation | alpha-Thalassemia - genetics | Electrophoresis, Capillary - methods | Prenatal Diagnosis - methods | Fetal Blood | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Nonimmune hydrops fetalis: identifying the underlying genetic etiology
by Sparks, Teresa N and Thao, Kao and Lianoglou, Billie R and Boe, Nina M and Bruce, Kari G and Datkhaeva, Ilina and Field, Nancy T and Fratto, Victoria M and Jolley, Jennifer and Laurent, Louise C and Mardy, Anne H and Murphy, Aisling M and Ngan, Emily and Rangwala, Naseem and Rottkamp, Catherine A. M and Wilson, Lisa and Wu, Erica and Uy, Cherry C and Valdez Lopez, Priscila and Norton, Mary E and Univ Calif Fetal Maternal Consorti and University of California Fetal–Maternal Consortium (UCfC) and on behalf of the University of California Fetal–Maternal Consortium (UCfC)
Genetics in medicine, ISSN 1098-3600, 06/2019, Volume 21, Issue 6, pp. 1339 - 1344
genetic | hydrops fetalis | diagnostic evaluation | nonimmune | etiology | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Humans | Aneuploidy | Male | California | Pregnancy Trimester, First | Pregnancy | Hydrops Fetalis - genetics | Ultrasonography, Prenatal | Adolescent | Adult | Female | Fetus | Retrospective Studies | Infant, Newborn | Cohort Studies | Hydrops Fetalis - etiology | Prenatal Care | Etiology | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Epidemiology of Live Born Infants with Nonimmune Hydrops Fetalis—Insights from a Population-Based Dataset
by Steurer, Martina A., MD, MAS and Peyvandi, Shabnam, MD and Baer, Rebecca J., MPH and MacKenzie, Tippi, MD and Li, Ben C., MD and Norton, Mary E., MD and Jelliffe-Pawlowski, Laura L., PhD and Moon-Grady, Anita J., MD
The Journal of pediatrics, ISSN 0022-3476, 2017, Volume 187, pp. 182 - 188.e3
Pediatrics | epidemiology | nonimmune hydrous fetalis | Life Sciences & Biomedicine | Science & Technology | Infant Mortality | Humans | Risk Factors | Hydrops Fetalis - mortality | Infant | Male | California | Gestational Age | Incidence | Pregnancy | Female | Hydrops Fetalis - epidemiology | Infant, Newborn | Databases, Factual | Dropsy | Edema | Infants | Epidemiology | Mortality | Infants (Newborn) | Genetic disorders | Analysis | Patient outcomes | Congenital heart disease | Heart diseases | Risk factors | Index Medicus | Abridged Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Nonimmune Hydrops Fetalis — More Than Meets the Eye?
by Kilby, Mark D
The New England journal of medicine, ISSN 0028-4793, 10/2020, Volume 383, Issue 18, pp. 1785 - 1786
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Usage | Genetic aspects | Diagnosis | Hydrops fetalis | Exome sequencing | Isoimmunization | Edema | Genotype & phenotype | Ultrasonic imaging | Phenotypes | Genetic disorders | Inborn errors of metabolism | Fetuses | Thorax | Metabolism | Peritoneum | Index Medicus | Abridged Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text A system‐based approach to the genetic etiologies of non‐immune hydrops fetalis
by Mardy, Anne H and Chetty, Shilpa P and Norton, Mary E and Sparks, Teresa N
Prenatal diagnosis, ISSN 0197-3851, 08/2019, Volume 39, Issue 9, pp. 732 - 750
Genetics & Heredity | Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Edema | Evaluation | Fetuses | Disorders | Karyotypes | Stenosis | Lysosomal storage diseases | Genetic screening | Gene sequencing | Ultrasonic imaging | DNA microarrays | Etiology | Hydrops fetalis | Diagnosis | Ultrasound | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text KLF1-null neonates display hydrops fetalis and a deranged erythroid transcriptome
by Magor, Graham W and Tallack, Michael R and Gillinder, Kevin R and Bell, Charles C and McCallum, Naomi and Williams, Bronwyn and Perkins, Andrew C
Blood, ISSN 0006-4971, 04/2015, Volume 125, Issue 15, pp. 2405 - 2417
Life Sciences & Biomedicine | Hematology | Science & Technology | Erythropoiesis | Humans | Anemia, Neonatal - complications | Erythroblasts - metabolism | Gene Expression Regulation | Transcriptome | Male | Hydrops Fetalis - blood | Hydrops Fetalis - pathology | Anemia, Neonatal - genetics | Autophagy | Hydrops Fetalis - genetics | Kruppel-Like Transcription Factors - metabolism | Gene Deletion | Anemia, Neonatal - blood | Female | Anemia, Neonatal - pathology | Kruppel-Like Transcription Factors - genetics | Infant, Newborn | Erythroblasts - pathology | Index Medicus | Abridged Index Medicus | Red Cells, Iron, and Erythropoiesis | 36
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights