Judith St. Onge: search on Z-Library

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1

Patient-centered care and patient safety: A model for nurse educators

St. Onge, Judith L., Parnell, Robin B.

Journal:

Teaching and Learning in Nursing

Year:

2015

Language:

english

File:

PDF, 250 KB

english, 2015

2

Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome

Vabres, Pierre, Sorlin, Arthur, Kholmanskikh, Stanislav S., Demeer, BÃ©nÃ©dicte, St-Onge, Judith, Duffourd, Yannis, Kuentz, Paul, Courcet, Jean-BenoÃ®t, Carmignac, Virginie, Garret, Philippine, Bessis

Journal:

Nature Genetics

Year:

2020

File:

PDF, 507 KB

2020

3

Teaching safety in nursing practice: Is emotional intelligence a vital component?

Parnell, Robin Brush, St. Onge, Judith L.

Journal:

Teaching and Learning in Nursing

Year:

2015

Language:

english

File:

PDF, 143 KB

english, 2015

4

Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome

Vabres, Pierre, Sorlin, Arthur, Kholmanskikh, Stanislav S., Demeer, Bénédicte, St-Onge, Judith, Duffourd, Yannis, Kuentz, Paul, Courcet, Jean-Benoît, Carmignac, Virginie, Garret, Philippine, Bessis, D

Journal:

Nature Genetics

Year:

2019

File:

PDF, 649 KB

2019

5

NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population

Julie Gauthier, Anna Bonnel, Judith St-Onge, Liliane Karemera, Sandra Laurent, Laurent Mottron, Éric Fombonne, Ridha Joober, Guy A. Rouleau

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2005

Language:

english

File:

PDF, 44 KB

english, 2005

6

Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and families

Lan Xiong, Patrick Dion, Jacques Montplaisir, Anastasia Levchenko, Pascale Thibodeau, Liliane Karemera, Jean-Baptiste Rivière, Judith St-Onge, Claudia Gaspar, Marie-Pierre Dubé, Alex Desautels, Gustav

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2007

Language:

english

File:

PDF, 86 KB

english, 2007

7

Novel de novo SHANK3 mutation in autistic patients

Julie Gauthier, Dan Spiegelman, Amélie Piton, Ronald G. Lafrenière, Sandra Laurent, Judith St-Onge, Line Lapointe, Fadi F. Hamdan, Patrick Cossette, Laurent Mottron, Éric Fombonne, Ridha Joober, Claud

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2009

Language:

english

File:

PDF, 207 KB

english, 2009

8

The 14q restless legs syndrome locus in the French Canadian population

Anastasia Levchenko, Jacques-Yves Montplaisir, Marie-Pierre Dubé, Jean-Baptiste Riviere, Judith St-Onge, Gustavo Turecki, Lan Xiong, Pascale Thibodeau, Alex Desautels, Dominique J. Verlaan, Guy A. Rou

Journal:

Annals of Neurology

Year:

2004

Language:

english

File:

PDF, 98 KB

english, 2004

9

Autosomal-dominant locus for restless legs syndrome in French-Canadians on chromosome 16p12.1

Anastasia Levchenko, Jacques-Yves Montplaisir, Géraldine Asselin, Sylvie Provost, Simon L. Girard, Lan Xiong, Emmanuelle Lemyre, Judith St-Onge, Pascale Thibodeau, Alex Desautels, Gustavo Turecki, Cla

Journal:

Movement Disorders

Year:

2009

Language:

english

File:

PDF, 308 KB

english, 2009

10

A Mutation that Creates a Pseudoexon in SOD1 Causes Familial ALS

Paul N. Valdmanis, Veronique V. Belzil, James Lee, Patrick A. Dion, Judith St-Onge, Pascale Hince, Benoit Funalot, Philippe Couratier, Pierre Clavelou, William Camu, Guy A. Rouleau

Journal:

Annals of Human Genetics

Year:

2009

Language:

english

File:

PDF, 230 KB

english, 2009

11

De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes

Rivière, Jean-Baptiste, Mirzaa, Ghayda M, O'Roak, Brian J, Beddaoui, Margaret, Alcantara, Diana, Conway, Robert L, St-Onge, Judith, Schwartzentruber, Jeremy A, Gripp, Karen W, Nikkel, Sarah M, Worthyl

Journal:

Nature Genetics

Year:

2012

Language:

english

File:

PDF, 1.08 MB

english, 2012

12

CAA insertion polymorphism in the 3′UTR of Nogo gene on 2p14 is not associated with schizophrenia

Lan Xiong, Guy A. Rouleau, Lynn E. DeLisi, Judith St-Onge, Robert Najafee, Jean-Baptiste Rivière, Chawki Benkelfat, Karim Tabbane, Ferid Fathalli, Zoltan Danics, Alain Labelle, Samarthji Lal, Ridha Jo

Journal:

Molecular Brain Research

Year:

2005

Language:

english

File:

PDF, 94 KB

english, 2005

13

Genetic association studies of neurotensin gene and restless legs syndrome in French Canadians

Lan Xiong, Anastasia Levchenko, Jacques Montplaisir, Jean-Baptiste Rivière, Pascale Thibodeau, Judith St-Onge, Claudia Gaspar, Alex Desautels, Paul Lespérance, Sylvain Chouinard, Gustavo Turecki, Guy

Journal:

Year:

2008

Language:

english

File:

PDF, 141 KB

english, 2008

14

Preventive practicum training in healthcare organizations: The Meharry model

Robert S Levine, Judith St. Onge, Cynthia J Moriarty, Stephanie Bailey, Thomas Logan, Kangmin Zhu, Bettie K Nelson, Richard A Hodder, William Marino

Journal:

American Journal of Preventive Medicine

Year:

1999

Language:

english

File:

PDF, 120 KB

english, 1999

15

PIK3R1 Mutations Cause Syndromic Insulin Resistance with Lipoatrophy

Thauvin-Robinet, Christel, Auclair, Martine, Duplomb, Laurence, Caron-Debarle, Martine, Avila, Magali, St-Onge, Judith, Le Merrer, Martine, Le Luyer, Bernard, Héron, Delphine, Mathieu-Dramard, Michèle

Journal:

The American Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 799 KB

english, 2013

16

Mutations in SLC13A5 Cause Autosomal-Recessive Epileptic Encephalopathy with Seizure Onset in the First Days of Life

Thevenon, Julien, Milh, Mathieu, Feillet, François, St-Onge, Judith, Duffourd, Yannis, Jugé, Clara, Roubertie, Agathe, Héron, Delphine, Mignot, Cyril, Raffo, Emmanuel, Isidor, Bertrand, Wahlen, Sandra

Journal:

The American Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 1.13 MB

english, 2014

17

Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis

Belzil, Véronique V, St-Onge, Judith, Daoud, Hussein, Desjarlais, Anne, Bouchard, Jean-Pierre, Dupré, Nicolas, Camu, William, Dion, Patrick A, Rouleau, Guy A

Journal:

Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 237 KB

english, 2011

18

Addictive Relationships and HIV Care

Onge, Judith L. St.

Journal:

Aids Patient Care

Year:

1992

Language:

english

File:

PDF, 598 KB

english, 1992

19

Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosis

Belzil, Veronique V., Daoud, Hussein, St-Onge, Judith, Desjarlais, Anne, Bouchard, Jean-Pierre, Dupre, Nicolas, Lacomblez, Lucette, Salachas, François, Pradat, Pierre-François, Meininger, Vincent, Cam

Journal:

Amyotrophic Lateral Sclerosis

Year:

2011

Language:

english

File:

PDF, 401 KB

english, 2011

20

Congenital neutropenia with retinopathy, a new phenotype without intellectual deficiency or obesity secondary to VPS 13 B mutations

Gueneau, Lucie, Duplomb, Laurence, Sarda, Pierre, Hamel, Christian, Aral, Bernard, Chehadeh, Salima El, Gigot, Nadège, St-Onge, Judith, Callier, Patrick, Thevenon, Julien, Huet, Frédéric, Carmignac, V

Journal:

American Journal of Medical Genetics Part A

Year:

2014

Language:

english

File:

PDF, 1.14 MB

english, 2014

21

An Innovative Tool for Experiential Learning of Nursing Quality and Safety Competencies

St. Onge, Judith, Hodges, &NA, Tracey, McBride, &NA, Marilyn, Parnell, Robin

Journal:

Year:

2013

Language:

english

File:

PDF, 169 KB

english, 2013

22

A Novel Duplication Confirms the Involvement of 5q23.2 in Autosomal Dominant Leukodystrophy

Meijer, Inge A., Simoes-Lopes, Ana A., Laurent, Sandra, Katz, Tanya, St-Onge, Judith, Verlaan, Dominique J., Dupré, Nicolas, Thibault, Manon, Mathurin, Johanne, Bouchard, Jean-Pierre, Rouleau, Guy A.

Journal:

Archives of Neurology

Year:

2008

Language:

english

File:

PDF, 204 KB

english, 2008

23

SELF-DISCLOSURE, ANXIETY, AND HEALTH WORRY IN UNSCHEDULED OUTPATIENTS

BYERS, PATRICIA H., ONGE, JUDITH L. ST., ATKINS, LOU ANN, PROKOP, JOHN A., GRAND, JOAN T.

Journal:

Psychological Reports

Year:

1988

Language:

english

File:

PDF, 298 KB

english, 1988

24

Association of Intronic Variants of the BTBD9 Gene With Tourette Syndrome

Rivière, Jean-Baptiste, Xiong, Lan, Levchenko, Anastasia, St-Onge, Judith, Gaspar, Claudia, Dion, Yves, Lespérance, Paul, Tellier, Geneviève, Richer, François, Chouinard, Sylvain, Rouleau, Guy A.

Journal:

Archives of Neurology

Year:

2009

Language:

english

File:

PDF, 193 KB

english, 2009

25

Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis

Thomas, Anna C., Zeng, Zhiqiang, Rivière, Jean-Baptiste, O’Shaughnessy, Ryan, Al-Olabi, Lara, St.-Onge, Judith, Atherton, David J., Aubert, Hélène, Bagazgoitia, Lorea, Barbarot, Sébastien, Bourrat, Em

Journal:

The Journal of Investigative Dermatology

Year:

2016

Language:

english

File:

PDF, 2.25 MB

english, 2016

26

SPG4 Founder Effect in French Canadians with Hereditary Spastic Paraplegia

Meijer, Inge A., Dupré, Nicolas, Brais, Bernard, Cossette, Patrick, St-Onge, Judith, Rioux, Marie-France, Benard, Melanie, Rouleau, Guy A.

Journal:

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

Year:

2007

File:

PDF, 78 KB

2007

27

Clinical Stringency Greatly Improves Mutation Detection in Rett Syndrome

Gauthier, Julie, Amorim, Giovana de, Mnatzakanian, Gevork N., Saunders, Carol, Vincent, John B., Toupin, Sylvie, Kauffman, David, St-Onge, Judith, Laurent, Sandra, Macleod, Patrick M., Minassian, Berg

Journal:

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

Year:

2005

File:

PDF, 100 KB

2005

28

Genome-Wide TDT Analysis in French-Canadian Families with Tourette Syndrome

Rivière, Jean-Baptiste, St-Onge, Judith, Gaspar, Claudia, Diab, Sabrina, Dion, Yves, Lespérance, Paul, Tellier, Geneviève, Richer, François, Chouinard, Sylvain, Dubé, Marie-Pierre, Rouleau, Guy A.

Journal:

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

Year:

2010

Language:

english

File:

PDF, 77 KB

english, 2010

29

Postzygotic BRAF p.Lys601Asn Mutation in Phacomatosis Pigmentokeratotica with Woolly Hair Nevus and Focal Cortical Dysplasia

Kuentz, Paul, Mignot, Cyril, St-Onge, Judith, Duffourd, Yannis, Bonniaud, Bertille, Faivre, Laurence, Rivière, Jean-Baptiste, Vabres, Pierre

Journal:

The Journal of Investigative Dermatology

Year:

2016

Language:

english

File:

PDF, 737 KB

english, 2016

30

Codependence: Addictive Relationships and HIV Care

St Onge, Judith L.

Journal:

Journal of Addictions Nursing

Year:

1991

Language:

english

File:

PDF, 456 KB

english, 1991

31

Application of whole-exome sequencing to unravel the molecular basis of undiagnosed syndromic congenital neutropenia with intellectual disability

Gauthier-Vasserot, Alexandra, Thauvin-Robinet, Christel, Bruel, Ange-Line, Duffourd, Yannis, St-Onge, Judith, Jouan, Thibaud, Rivière, Jean-Baptiste, Heron, Delphine, Donadieu, Jean, Bellanné-Chantelo

Journal:

American Journal of Medical Genetics Part A

Year:

2016

Language:

english

File:

PDF, 139 KB

english, 2016

32

Molecular diagnosis of PIK3CA-related overgrowth spectrum (PROS) in 162 patients and recommendations for genetic testing

Kuentz, Paul, St-Onge, Judith, Duffourd, Yannis, Courcet, Jean-Benoît, Carmignac, Virginie, Jouan, Thibaud, Sorlin, Arthur, Abasq-Thomas, Claire, Albuisson, Juliette, Amiel, Jeanne, Amram, Daniel, Arp

Journal:

Genetics in Medicine

Year:

2017

Language:

english

File:

PDF, 808 KB

english, 2017

33

Mosaicism for a KITLG mutation in linear and whorled nevoid hypermelanosis

Sorlin, Arthur, Maruani, Annabel, Aubriot-Lorton, Marie-Hélène, Kuentz, Paul, Duffourd, Yannis, Teysseire, Sandra, Carmignac, Virginie, St-Onge, Judith, Chevarin, Martin, Jouan, Thibaud, Thauvin-Robin

Journal:

The Journal of Investigative Dermatology

Year:

2017

File:

PDF, 1.73 MB

2017

34

Bilateral nail gun traumatic brain injury presents as intentional overdose: A case report

Alain, Judith, Lavergne, Pascal, St-Onge, Maude, D’Astous, Myreille, Côté, Stéphane

Journal:

Year:

2017

File:

PDF, 479 KB

2017

35

BET 3: In septic patients requiring fluid resuscitation can the bedside lung ultrasound be used to assess the pulmonary fluid status?

Judith, Alain, St-Onge, Maude

Journal:

Emergency Medicine Journal

Year:

2017

Language:

english

File:

PDF, 104 KB

english, 2017

36

Expanding the clinical spectrum of recessive truncating mutations of KLHL7 to a Bohring-Opitz-like phenotype

Bruel, Ange-Line, Bigoni, Stefania, Kennedy, Joanna, Whiteford, Margo, Buxton, Chris, Parmeggiani, Giulia, Wherlock, Matt, Woodward, Geoff, Greenslade, Mark, Williams, Maggie, St-Onge, Judith, Ferlini

Journal:

Journal of Medical Genetics

Year:

2017

Language:

english

File:

PDF, 526 KB

english, 2017

37

Pathogenic variants in AIMP1 cause pontocerebellar hypoplasia

Accogli, Andrea, Russell, Laura, Sébire, Guillaume, Rivière, Jean-Baptiste, St-Onge, Judith, Addour-Boudrahem, Nassima, Laporte, Alexandre Dionne, Rouleau, Guy A., Saint-Martin, Christine, Srour, Myri

Journal:

Year:

2019

Language:

english

File:

PDF, 347 KB

english, 2019

38

Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome

Vabres, Pierre, Sorlin, Arthur, Kholmanskikh, Stanislav S., Demeer, Bénédicte, St-Onge, Judith, Duffourd, Yannis, Kuentz, Paul, Courcet, Jean-Benoît, Carmignac, Virginie, Garret, Philippine, Bessis, D

Journal:

Nature Genetics

Year:

2019

Language:

english

File:

PDF, 1.81 MB

english, 2019

39

De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Collosum, Axon, Cardiac, Ocular, and Genital Defects

Accogli, Andrea, Calabretta, Sara, St-Onge, Judith, Boudrahem-Addour, Nassima, Dionne-Laporte, Alexandre, Joset, Pascal, Azzarello-Burri, Silvia, Rauch, Anita, Krier, Joel, Fieg, Elizabeth, Pallais, J

Journal:

The American Journal of Human Genetics

Year:

2019

Language:

english

File:

PDF, 1.68 MB

english, 2019

40

Heterozygous Missense Pathogenic Variants Within the Second Spectrin Repeat of SPTBN2 Lead to Infantile-Onset Cerebellar Ataxia

Accogli, Andrea, St-Onge, Judith, Addour-Boudrahem, Nassima, Lafond-Lapalme, Joël, Laporte, Alexandre Dionne, Rouleau, Guy A., Rivière, Jean-Baptiste, Srour, Myriam

Journal:

Journal of Child Neurology

Year:

2019

Language:

english

File:

PDF, 271 KB

english, 2019

41

De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Collosum, Axon, Cardiac, Ocular, and Genital Defects

Accogli, Andrea, Calabretta, Sara, St-Onge, Judith, Boudrahem-Addour, Nassima, Dionne-Laporte, Alexandre, Joset, Pascal, Azzarello-Burri, Silvia, Rauch, Anita, Krier, Joel, Fieg, Elizabeth, Pallais, J

Journal:

The American Journal of Human Genetics

Year:

2019

File:

PDF, 1.68 MB

2019

42

Heterozygous Missense Pathogenic Variants Within the Second Spectrin Repeat of SPTBN2 Lead to Infantile-Onset Cerebellar Ataxia

Accogli, Andrea, St-Onge, Judith, Addour-Boudrahem, Nassima, Lafond-Lapalme, Joël, Laporte, Alexandre Dionne, Rouleau, Guy A., Rivière, Jean-Baptiste, Srour, Myriam

Journal:

Journal of Child Neurology

Year:

2019

File:

PDF, 271 KB

2019

43

Self-Care Styles in Military Veterans

Onge, Judith L. St.

Journal:

Military Medicine

Year:

1995

Language:

english

File:

PDF, 847 KB

english, 1995

44

Self-Care Styles in Military Veterans

Onge, Judith L. St.

Journal:

Military Medicine

Year:

1995

File:

PDF, 847 KB

1995

45

Severe DNM1 encephalopathy with dysmyelination due to recurrent splice site pathogenic variant

Sahly, Ahmed N., Krochmalnek, Eric, St-Onge, Judith, Srour, Myriam, Myers, Kenneth A.

Journal:

Year:

2020

File:

PDF, 612 KB

2020

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