X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (97) 97
Publication (11) 11
Newspaper Article (6) 6
Web Resource (5) 5
Conference Proceeding (2) 2
Book / eBook (1) 1
Book Chapter (1) 1
Book Review (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (43) 43
index medicus (40) 40
female (34) 34
male (32) 32
child, preschool (22) 22
clinical neurology (22) 22
jordan (22) 22
infant (18) 18
child (17) 17
mutation (16) 16
children (14) 14
genetics & heredity (14) 14
adolescent (12) 12
consanguinity (12) 12
pediatrics (11) 11
pedigree (11) 11
epilepsy (10) 10
retrospective studies (10) 10
article (9) 9
genetic aspects (9) 9
neurosciences (9) 9
animals (8) 8
disease (8) 8
neurology (8) 8
genetic disorders (7) 7
health aspects (7) 7
homozygote (7) 7
mutations (7) 7
research (7) 7
adult (6) 6
gene mutations (6) 6
phenotype (6) 6
proteins (6) 6
risk factors (6) 6
startle disease (6) 6
syndrome (6) 6
analysis (5) 5
biochemistry & molecular biology (5) 5
case-control studies (5) 5
follow-up studies (5) 5
genetics (5) 5
genotype & phenotype (5) 5
hospitals (5) 5
infant, newborn (5) 5
jordan - epidemiology (5) 5
magnetic resonance imaging (5) 5
medical research (5) 5
mice (5) 5
patients (5) 5
population (5) 5
receptors, glycine - genetics (5) 5
seizures (5) 5
subunit (5) 5
surgery (5) 5
zebrafish (5) 5
brain - pathology (4) 4
case report (4) 4
children & youth (4) 4
development and progression (4) 4
dna mutational analysis (4) 4
gene (4) 4
genes, recessive (4) 4
genes, recessive - genetics (4) 4
genetic research (4) 4
genomes (4) 4
hyperekplexia (4) 4
inhibitory glycine receptor (4) 4
international education (4) 4
medicine, experimental (4) 4
molecular sequence data (4) 4
neurological disorders (4) 4
physiological aspects (4) 4
poisoning (4) 4
young adult (4) 4
age (3) 3
amino acid sequence (3) 3
anticonvulsants - therapeutic use (3) 3
article subject (3) 3
care and treatment (3) 3
chloride channels (3) 3
colleges & universities (3) 3
cytogenetics (3) 3
developmental disabilities - genetics (3) 3
diagnosis (3) 3
enzymes (3) 3
epilepsy - diagnosis (3) 3
epilepsy - genetics (3) 3
exome sequencing (3) 3
families & family life (3) 3
family health (3) 3
fatal outcome (3) 3
foreign students (3) 3
genes (3) 3
genotype (3) 3
glycine plasma membrane transport proteins - genetics (3) 3
glycine receptors (3) 3
identification and classification (3) 3
infants (3) 3
international students (3) 3
medicine (3) 3
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Pediatric Neurology, ISSN 1304-2580, 03/2006, Volume 4, Issue 1, pp. 049 - 051
Abstract Abnormal movements including tremor and myoclonus have been described in patients with vitamin B12 deficiency before or upon initiation of treatment... 
Case Report | Eye myoclonus | Abnormal movements | Tremor | Vitamin B12 | Babies | Vitamin deficiency | Eye movements | Vitamin B | Neurological disorders
Journal Article
Journal of Pediatric Neurology, ISSN 1304-2580, 12/2006, Volume 4, Issue 4, pp. 245 - 249
Abstract We aimed to determine the incidence, types of neural tube defects (NTDs), seasonal variation, complications, and follow up of a sample of children... 
Original Article | Anencephaly | Myelomeningocele | Jordan | Neural tube defects | Medical research | Birth defects | Nutrition | Vitamin B | Children & youth
Journal Article
Science, ISSN 0036-8075, 2014, Volume 343, Issue 6170, pp. 506 - 511
Journal Article
Higher Education Policy, ISSN 0952-8733, 12/2016, Volume 29, Issue 4, p. 539
In 2014, the Canadian federal government announced its first-ever international education strategy. Referencing Cerna’s ( 2014 ) typology of interactions... 
Federal government | Landscape | International education | Higher education | Organizational change | Globalization | Colleges & universities | College students | Typology | Public policy | Recruitment
Journal Article
Brain & Development, ISSN 0387-7604, 2015, Volume 38, Issue 2, pp. 204 - 208
Journal Article
Journal of Pediatric Neurology, ISSN 1304-2580, 06/2011, Volume 9, Issue 2, pp. 203 - 208
Abstract Paroxysmal non-epileptic disorders (PNEDs) are often misdiagnosed as epilepsy. This study describes cases of misdiagnosed PNEDs. In addition, it... 
vasovagal syncope | Paroxysmal non-epileptic events | breath-holdings spells | hyperekplexia | masturbation | mobile phone | Epilepsy | Migraine | Families & family life | Headaches | Electroencephalography | Medical diagnosis | Patients | Children & youth | Sleep | Cellular telephones | Cameras | Digital video | Age
Journal Article
Higher Education Policy, ISSN 0952-8733, 12/2016, Volume 29, Issue 4, pp. 539 - 563
In 2014, the Canadian federal government announced its first-ever international education strategy. Referencing Cerna's (2014) typology of interactions between... 
internationalization | international education strategy | institutional policy | international students and immigration | international students | SYSTEM | EDUCATION & EDUCATIONAL RESEARCH | STATE | UNIVERSITIES
Journal Article
Globalisation, Societies and Education, ISSN 1476-7724, 10/2017, Volume 15, Issue 5, pp. 666 - 678
In Canada's first-ever strategy, international education (IE) is linked to immigration policy with international students (IS) recruited as 'ideal' immigrants.... 
immigration | recruitment and retention of international students | International students | labour market | competition for skilled migrants | international education policy | Legitimation | International education | Critical theory | Immigration policy | Ideology | Discourse analysis | Foreign students | Power
Journal Article
Journal of Pediatric Neurology, ISSN 1304-2580, 06/2006, Volume 4, Issue 2, pp. 143 - 146
Abstract Canavan disease (CD) is a fatal, hereditary disorder of central nervous system development that has been linked to mutations in the gene for the... 
Case Report | Canavan disease | Leukodystrophy | Macrocephaly | Urine | Parents & parenting | Birth weight | Mutation | History | Patients | Neurological disorders
Journal Article
Neuron, ISSN 0896-6273, 12/2014, Volume 84, Issue 6, pp. 1240 - 1257
Journal Article
by Braun, Daniela A and Rao, Jia and Mollet, Geraldine and Schapiro, David and Daugeron, Marie-Claire and Tan, Weizhen and Gribouval, Olivier and Boyer, Olivia and Revy, Patrick and Jobst-Schwan, Tilman and Schmidt, Johanna Magdalena and Lawson, Jennifer A and Schanze, Denny and Ashraf, Shazia and Ullmann, Jeremy F P and Hoogstraten, Charlotte A and Boddaert, Nathalie and Collinet, Bruno and Martin, Gaëlle and Liger, Dominique and Lovric, Svjetlana and Furlano, Monica and Guerrera, I Chiara and Sanchez-Ferras, Oraly and Hu, Jennifer F and Boschat, Anne-Claire and Sanquer, Sylvia and Menten, Björn and Vergult, Sarah and De Rocker, Nina and Airik, Merlin and Hermle, Tobias and Shril, Shirlee and Widmeier, Eugen and Gee, Heon Yung and Choi, Won-Il and Sadowski, Carolin E and Pabst, Werner L and Warejko, Jillian K and Daga, Ankana and Basta, Tamara and Matejas, Verena and Scharmann, Karin and Kienast, Sana D and Behnam, Babak and Beeson, Brendan and Begtrup, Amber and Bruce, Malcolm and Ch'ng, Gaik-Siew and Lin, Shuan-Pei and Chang, Jui-Hsing and Chen, Chao-Huei and Cho, Megan T and Gaffney, Patrick M and Gipson, Patrick E and Hsu, Chyong-Hsin and Kari, Jameela A and Ke, Yu-Yuan and Kiraly-Borri, Cathy and Lai, Wai-Ming and Lemyre, Emmanuelle and Littlejohn, Rebecca Okashah and Masri, Amira and Moghtaderi, Mastaneh and Nakamura, Kazuyuki and Ozaltin, Fatih and Praet, Marleen and Prasad, Chitra and Prytula, Agnieszka and Roeder, Elizabeth R and Rump, Patrick and Schnur, Rhonda E and Shiihara, Takashi and Sinha, Manish D and Soliman, Neveen A and Soulami, Kenza and Sweetser, David A and Tsai, Wen-Hui and Tsai, Jeng-Daw and Topaloglu, Rezan and Vester, Udo and Viskochil, David H and Vatanavicharn, Nithiwat and Waxler, Jessica L and Wierenga, Klaas J and Wolf, Matthias T F and Wong, Sik-Nin and Leidel, Sebastian A and Truglio, Gessica and Dedon, Peter C and Poduri, Annapurna and Mane, Shrikant and Lifton, Richard P and Bouchard, Maxime and Kannu, Peter and Chitayat, David and Magen, Daniella and Callewaert, Bert and van Tilbeurgh, Herman and Zenker, Martin and ...
Nature Genetics, ISSN 1061-4036, 2017, Volume 49, Issue 10, pp. 1529 - 1529
Galloway-Mowat syndrome (GAMOS) is an autosomal-recessive disease characterized by the combination of early-onset nephrotic syndrome (SRNS) and microcephaly... 
YEAST | UNFOLDED PROTEIN RESPONSE | TRANSFER-RNA MODIFICATION | DNA | KINASE | GENETICS & HEREDITY | SECKEL-SYNDROME | GENOME MAINTENANCE | WDR73 | GALLOWAY-MOWAT SYNDROME | MASS-SPECTROMETRY | Metalloendopeptidases - genetics | Protein-Serine-Threonine Kinases - deficiency | Microcephaly - genetics | Humans | Metalloendopeptidases - deficiency | Apoptosis - genetics | Multiprotein Complexes - genetics | Nephrotic Syndrome - genetics | DNA Repair - genetics | Telomere Homeostasis - genetics | Endoplasmic Reticulum Stress - genetics | Intracellular Signaling Peptides and Proteins - deficiency | Hernia, Hiatal - genetics | Intracellular Signaling Peptides and Proteins - genetics | Podocytes - metabolism | RNA, Transfer - metabolism | Protein-Serine-Threonine Kinases - genetics | Models, Molecular | Nephrotic Syndrome - pathology | Zebrafish | Cytoskeleton - ultrastructure | Nephrosis - genetics | Gene Knockout Techniques | Carrier Proteins - genetics | Podocytes - ultrastructure | Zebrafish Proteins - deficiency | Animals | RNA Processing, Post-Transcriptional - genetics | CRISPR-Cas Systems | Protein Conformation | Mice | Mutation | Zebrafish Proteins - genetics | Cell Movement | Genetic disorders | Gene mutations | Development and progression | Nephrotic syndrome | Genetic aspects | Microcephaly | Health aspects | Cell proliferation | Brain | CRISPR | Genes | DNA damage | Genomes | Lethality | Kinases | Proteins | Genotype & phenotype | Microencephaly | Actin | Biopsy | Cytoskeleton | Scientific imaging | Endoplasmic reticulum | Mass spectrometry | Deoxyribonucleic acid--DNA | Apoptosis | Life Sciences
Journal Article
Nature Genetics, ISSN 1061-4036, 05/2015, Volume 47, Issue 5, pp. 528 - 534
Journal Article
Nature Genetics, ISSN 1061-4036, 09/2009, Volume 41, Issue 9, pp. 1016 - 1021
Journal Article