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Search Articles for "Prader-Willi Syndrome"

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Treatment of scoliosis in patients affected with Prader-Willi syndrome using various techniques

Author(s): Greggi Tiziana | Martikos Konstantinos | Lolli Francesco | Bakaloudis Georgios | Di Silvestre Mario | Cioni Alfredo | Bròdano Giovanni | Giacomini Stefano
Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder

Author(s): Delorme Richard | Moreno-De-Luca Daniel | Gennetier Aurélie | Maier Wolfgang | Chaste Pauline | Mössner Rainald | Grabe Hans | Ruhrmann Stephan | Falkai Peter | Mouren Marie-Christine | Leboyer Marion | Wagner Michael | Betancur Catalina
Anesthesia for Pediatric Patients with Prader-Willi Syndrome: Report of Two Cases

Author(s): Chi-Hao Tseng | Chit Chen | Chung-Hang Wong | Shu-Yam Wong | Kit-Man Wong
Different anaesthetic problems in Prader-Willi Syndrome

Author(s): V. Moschini | G. Marra | S. Elia
Childhood obesity: Referred cases to a tertiary health center in Riyadh, Saudi Arabia

Author(s): Al Herbish Abdullah | Al Jurayyan Nasir | Olasope Abiodun | Abdullah Asaad | Al Nuaim Abdulrahman
Practice guidelines for the molecular analysis of Prader-Willi and Angelman syndromes

Author(s): Ramsden Simon | Clayton-Smith Jill | Birch Rachael | Buiting Karin
French database of children and adolescents with Prader-Willi syndrome

Author(s): Molinas Catherine | Cazals Laurent | Diene Gwenaelle | Glattard Melanie | Arnaud Catherine | Tauber Maithe
Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: Efficient identification of known microduplications and identification of a novel microduplication in ASMT

Author(s): Cai Guiqing | Edelmann Lisa | Goldsmith Juliet | Cohen Ninette | Nakamine Alisa | Reichert Jennifer | Hoffman Ellen | Zurawiecki Danielle | Silverman Jeremy | Hollander Eric | Soorya Latha | Anagnostou Evdokia | Betancur Catalina | Buxbaum Joseph
Distal Xq duplication and functional Xq disomy

Author(s): Sanlaville Damien | Schluth-Bolard Caroline | Turleau Catherine
Strength characterization of knee flexor and extensor muscles in Prader-Willi and obese patients

Author(s): Capodaglio Paolo | Vismara Luca | Menegoni Francesco | Baccalaro Gabriele | Galli Manuela | Grugni Graziano
Cognitive profiles of genetic syndromes with Intellectual Disability

Author(s): Di Nuovo, Santo | Buono, Serafino
Gait patterns in Prader-Willi and Down syndrome patients

Author(s): Cimolin Veronica | Galli Manuela | Grugni Graziano | Vismara Luca | Albertini Giorgio | Rigoldi Chiara | Capodaglio Paolo
Top-down or bottom-up: Contrasting perspectives on psychiatric diagnoses

Author(s): Willem MA Verhoeven | Siegfried Tuinier | Ineke van der Burgt
Developmental Profiles and Mentality in Preschool Children with Prader-Willi Syndrome: A Preliminary Study

Author(s): Chien-Min Chen | Chia-Ling Chen | Jia-Woei Hou | Hung-Chih Hsu | Chia-Ying Chung | Shih-Wei Chou | Chu-Hsu Lin | Kai-Hua Chen
Prader-Willi syndrome: Methylation study or fluorescence in situ hybridization first?

Author(s): Hamzi Khalil | Itto Afaf | Nassereddine Sanaa | Nadifi Sellama
Effect of crowth hormone on muscle strength, tone and mobility of children with Prader-Willi syndrome

Author(s): Shadab SALEHPOUR | Farzaneh Rohani | Omid ARYANI | Massoud HOUSHMAND | Farhad HASHEMINEZHAD | Morteza REZVANI KASHANI | Farhad MAHVELATI SHAMSABADI | Zahra POURNASIRI
A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect

Author(s): De Molfetta Greice Andreotti | Felix Temis Maria | Riegel Mariluce | Ferraz Victor Evangelista de Faria | Pina Neto João Monteiro de
Diagnosis of patients with Prader-Willi and Angelman Syndromes: the importance of an overall investigation

Author(s): Varela Monica Castro | Fridman Cintia | Koiffmann Célia Priszkulnik
Phenotypic and behavioral variability within Angelman Syndrome group with UPD

Author(s): Fridman Cintia | Varela Monica C. | Valente Kette | Marques-Dias Maria J. | Koiffmann Célia P.
The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene

Author(s): Watrin Françoise | Le Meur Elodie | Roeckel Nathalie | Ripoche Marie-Anne | Dandolo Luisa | Muscatelli Françoise
Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome

Author(s): Schüle Birgitt | Albalwi Mohammed | Northrop Emma | Francis David | Rowell Margaret | Slater Howard | Gardner RJ McKinlay | Francke Uta
Genetic mapping of putative Chrna7 and Luzp2 neuronal transcriptional enhancers due to impact of a transgene-insertion and 6.8 Mb deletion in a mouse model of Prader-Willi and Angelman syndromes

Author(s): Stefan Mihaela | Claiborn Kathryn | Stasiek Edyta | Chai Jing-Hua | Ohta Tohru | Longnecker Richard | Greally John | Nicholls Robert
Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death

Author(s): Andrieu David | Meziane Hamid | Marly Fabienne | Angelats Corinne | Fernandez Pierre-Alain | Muscatelli Françoise
Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15

Author(s): Wang Nicholas | Parokonny Alexander | Thatcher Karen | Driscoll Jennette | Malone Barbara | Dorrani Naghmeh | Sigman Marian | LaSalle Janine | Schanen N Carolyn
Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region

Author(s): Jiang Yong-hui | Wauki Kekio | Liu Qian | Bressler Jan | Pan Yanzhen | Kashork Catherine | Shaffer Lisa | Beaudet Arthur
Deletion 22q13.3 syndrome

Author(s): Phelan Mary
DIAGNOSIS AND TREATMENT OF DEPRESSION IN PERSONS WITH INTELLECTUAL DISABILITY

Author(s): Katarina Tomić1, | Goran Mihajlović2, | Natalija Jovanović Mihajlović3 | Slavica Đukić Dejanović2, and | Katarina Mihajlović4 | Goran Petrović2
Fractal dimension approach in postural control of subjects with Prader-Willi Syndrome

Author(s): Cimolin Veronica | Galli Manuela | Rigoldi Chiara | Grugni Graziano | Vismara Luca | Mainardi Luca | Capodaglio Paolo
Prader-Willi syndrome: A primer for clinicians

Author(s): Cataletto Mary | Angulo Moris | Hertz Gila | Whitman Barbara
Periodontal disease in a patient with Prader-Willi syndrome: a case report

Author(s): Yanagita Manabu | Hirano Hiroyuki | Kobashi Mariko | Nozaki Takenori | Yamada Satoru | Kitamura Masahiro | Murakami Shinya
Complex chromosome rearrangements related 15q14 microdeletion plays a relevant role in phenotype expression and delineates a novel recurrent syndrome

Author(s): Roberti Maria | Surace Cecilia | Digilio Maria | D'Elia Gemma | Sirleto Pietro | Capolino Rossella | Lombardo Antonietta | Tomaiuolo Anna | Petrocchi Stefano | Angioni Adriano
Postural adaptations to long-term training in Prader-Willi patients

Author(s): Capodaglio Paolo | Cimolin Veronica | Vismara Luca | Grugni Graziano | Parisio Cinzia | Sibilia Olivia | Galli Manuela
Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients with Prader-Willi syndrome: a randomised placebo-controlled trial in 24 patients

Author(s): Tauber Maïthe | Mantoulan Carine | Copet Pierre | Jauregui Joseba | Demeer Genevieve | Diene Gwenaëlle | Rogé Bernadette | Laurier Virginie | Ehlinger Virginie | Arnaud Catherine | Molinas Catherine | Thuilleaux Denise

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