Found: 96
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The Ocean Hill–Brownsville Conflict: Intellectual Struggles between Blacks and Jews at Mid-century.
- Published in:
- 2013
- By:
- Publication type:
- Book Review
American Pogrom: The East St. Louis Race Riot and Black Politics.
- Published in:
- 2009
- By:
- Publication type:
- Book Review
Many Minds, One Heart: SNCC's Dream for a New America.
- Published in:
- 2007
- By:
- Publication type:
- Book Review
Enter the New Negroes: Images of Race in American Culture.
- Published in:
- 2005
- By:
- Publication type:
- Book Review
Julius Rosenwald: Repairing the World by Hasia R. Diner (review).
- Published in:
- 2019
- By:
- Publication type:
- Book Review
Julius Rosenwald: Repairing the World by Hasia R. Diner (review).
- Published in:
- 2019
- By:
- Publication type:
- Book Review
Crown Heights: Blacks, Jews, and the 1991 Brooklyn Riot.
- Published in:
- 2007
- By:
- Publication type:
- Book Review
Two novel mutations in a Canadian family with aspartylglucosaminuria and early outcome post bone marrow transplantation.
- Published in:
- Clinical Genetics, 1997, v. 51, n. 3, p. 174, doi. 10.1111/j.1399-0004.1997.tb02448.x
- By:
- Publication type:
- Article
Experiences of caregivers of children with inherited metabolic diseases: a qualitative study.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Experiences of caregivers of children with inherited metabolic diseases: a qualitative study.
- Published in:
- Orphanet Journal of Rare Diseases, 2016, v. 11, p. 1, doi. 10.1186/s13023-016-0548-2
- By:
- Publication type:
- Article
The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Assessing the quality and value of metabolic chart data for capturing core outcomes for pediatric medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.
- Published in:
- BMC Pediatrics, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12887-023-04393-4
- By:
- Publication type:
- Article
Book reviews.
- Published in:
- 1993
- By:
- Publication type:
- Book Review
New insights into the landscape of ALPL gene variants in patients with hypophosphatasia from the Global HPP Registry.
- Published in:
- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 11, p. 1, doi. 10.1002/ajmg.a.63781
- By:
- Publication type:
- Article
Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Survival of fetuses with abnormal karyotypes and cystic hygromas detected prenatally.
- Published in:
- Prenatal Diagnosis, 1990, v. 10, n. 2, p. 136, doi. 10.1002/pd.1970100213
- By:
- Publication type:
- Article
The BOR syndrome and renal agenesis-prenatal diagnosis andfurther clinical delineation.
- Published in:
- Prenatal Diagnosis, 1988, v. 8, n. 2, p. 103, doi. 10.1002/pd.1970080204
- By:
- Publication type:
- Article
Clinical Profiles of Children with Hypophosphatasia prior to Treatment with Enzyme Replacement Therapy: An Observational Analysis from the Global HPP Registry.
- Published in:
- Hormone Research in Paediatrics, 2024, v. 97, n. 3, p. 233, doi. 10.1159/000531865
- By:
- Publication type:
- Article
Newborn screening by tandem mass spectrometry: ethical and social issues.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Oral Language Development in a Child With Floating-Harbor Syndrome.
- Published in:
- Language, Speech & Hearing Services in Schools, 1999, v. 30, n. 2, p. 207, doi. 10.1044/0161-1461.3002.207
- By:
- Publication type:
- Article
A large novel deletion in the APC promoter region causes gene silencing and leads to classical familial adenomatous polyposis in a Manitoba Mennonite kindred.
- Published in:
- Human Genetics, 2008, v. 124, n. 5, p. 535, doi. 10.1007/s00439-008-0579-4
- By:
- Publication type:
- Article
Family‐centred care interventions for children with chronic conditions: A scoping review.
- Published in:
- Health Expectations, 2024, v. 27, n. 1, p. 1, doi. 10.1111/hex.13897
- By:
- Publication type:
- Article
Impact of muscular symptoms and/or pain on disease characteristics, disability, and quality of life in adult patients with hypophosphatasia: A cross-sectional analysis from the Global HPP Registry.
- Published in:
- Frontiers in Endocrinology, 2023, v. 14, p. 1, doi. 10.3389/fendo.2023.1138599
- By:
- Publication type:
- Article
Neonatal hypoglycemia and the CPT1A P479L variant in term newborns: A retrospective cohort study of Inuit newborns from Kivalliq Nunavut.
- Published in:
- Paediatrics & Child Health (1205-7088), 2021, v. 26, n. 4, p. 218, doi. 10.1093/pch/pxaa039
- By:
- Publication type:
- Article
Social paediatrics: From 'lip service' to the health and well-being of Canada's children and youth.
- Published in:
- Paediatrics & Child Health (1205-7088), 2013, v. 18, n. 7, p. 351
- By:
- Publication type:
- Article
Hutterite brothers both affected with two forms of limb girdle muscular dystrophy: LGMD2H and LGMD2I.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 8, p. 978, doi. 10.1038/sj.ejhg.5201436
- By:
- Publication type:
- Article
Effectiveness of asfotase alfa for treatment of adults with hypophosphatasia: results from a global registry.
- Published in:
- Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03048-6
- By:
- Publication type:
- Article
Diagnostic delay is common among patients with hypophosphatasia: initial findings from a longitudinal, prospective, global registry.
- Published in:
- 2019
- By:
- Publication type:
- journal article
An insight into the mechanisms of COVID-19, SARS-CoV2 infection severity concerning β-cell survival and cardiovascular conditions in diabetic patients.
- Published in:
- Molecular & Cellular Biochemistry, 2022, v. 477, n. 6, p. 1681, doi. 10.1007/s11010-022-04396-2
- By:
- Publication type:
- Article
Prenatal onset of the neuroradiologic phenotype of pyruvate carboxylase deficiency due to homozygous PC c.1828G > A mutations.
- Published in:
- Journal of Inherited Metabolic Disease Reports, 2021, v. 61, n. 1, p. 42, doi. 10.1002/jmd2.12235
- By:
- Publication type:
- Article
Textbook Treatments of the Roles of Ritual and Women in Judaism.
- Published in:
- Jewish Social Studies, 1984, v. 46, n. 1, p. 73
- By:
- Publication type:
- Article
Identifying Non-Duchenne Muscular Dystrophy-Positive and False Negative Results in Prior Duchenne Muscular Dystrophy Newborn Screening Programs.
- Published in:
- JAMA Neurology, 2016, v. 73, n. 1, p. 111, doi. 10.1001/jamaneurol.2015.3537
- By:
- Publication type:
- Article
A Concise History of American Antisemitism.
- Published in:
- 2007
- By:
- Publication type:
- Book Review
Trends in Telehealth versus On-site Clinical Genetics Appointments in Manitoba: A Comparative Study.
- Published in:
- Journal of Genetic Counseling, 2012, v. 21, n. 2, p. 337, doi. 10.1007/s10897-011-9406-5
- By:
- Publication type:
- Article
Genetic Counseling in a Busy Pediatric Metabolic Practice.
- Published in:
- Journal of Genetic Counseling, 2011, v. 20, n. 1, p. 20, doi. 10.1007/s10897-010-9324-y
- By:
- Publication type:
- Article
Mennonites, Hypophosphatasia and Severe Combined Immunodeficiency Disease: The Story of Two Genetic Disorders.
- Published in:
- Journal of Mennonite Studies, 2016, v. 34, p. 89
- By:
- Publication type:
- Article
Clinical profiles of treated and untreated adults with hypophosphatasia in the Global HPP Registry.
- Published in:
- Orphanet Journal of Rare Diseases, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s13023-022-02393-8
- By:
- Publication type:
- Article
Clinical profiles of treated and untreated adults with hypophosphatasia in the Global HPP Registry.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Neuropathological, biochemical and molecular findings in a glutaric acidemia type 1 cohort.
- Published in:
- 2005
- By:
- Publication type:
- journal article
Neuropathological, biochemical and molecular findings in a glutaric acidemia type 1 cohort.
- Published in:
- Brain: A Journal of Neurology, 2005, v. 128, n. 4, p. 711
- By:
- Publication type:
- Article
The prevalence of the HNF-1alpha G319S mutation in Canadian aboriginal youth with type 2 diabetes.
- Published in:
- 2002
- By:
- Publication type:
- journal article
The C677T methylenetetrahydrofolate reductase variant and third trimester obstetrical complications in women with unexplained elevations of maternal serum alpha-fetoprotein.
- Published in:
- Reproductive Biology & Endocrinology, 2004, v. 2, p. 65, doi. 10.1186/1477-7827-2-65
- By:
- Publication type:
- Article
Caffeine is a risk factor for osteopenia of prematurity in preterm infants: a cohort study.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Eugenic abortion: an ethical critique.
- Published in:
- Canadian Medical Association Journal (CMAJ), 1991, v. 144, n. 1, p. 8
- By:
- Publication type:
- Article
Homelands (Book).
- Published in:
- 2003
- By:
- Publication type:
- Book Review
Newborn Screening for IKBKB Deficiency in Manitoba, Using Genetic Mutation Analysis.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Evaluation of the quality of clinical data collection for a pan-Canadian cohort of children affected by inherited metabolic diseases: lessons learned from the Canadian Inherited Metabolic Diseases Research Network.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Cardiac and respiratory failure in limb‐girdle muscular dystrophy 2I.
- Published in:
- Annals of Neurology, 2004, v. 56, n. 5, p. 738
- By:
- Publication type:
- Article
Causes and risk factors for infant mortality in Nunavut, Canada 1999-2011.
- Published in:
- BMC Pediatrics, 2012, v. 12, n. 1, p. 190, doi. 10.1186/1471-2431-12-190
- By:
- Publication type:
- Article
Correction to: Does specialist physician supply affect pediatric asthma health outcomes?
- Published in:
- 2019
- By:
- Publication type:
- corrected article