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Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome.
Boot, Erik; Óskarsdóttir, Sólveig; Loo, Joanne C Y; Crowley, Terrence Blaine; Orchanian-Cheff, Ani; Andrade, Danielle M; Arganbright, Jill M; Castelein, René M; Cserti-Gazdewich, Christine; de Reuver, Steven; Fiksinski, Ania M; Klingberg, Gunilla; Lang, Anthony E; Mascarenhas, Maria R; Moss, Edward M; Nowakowska, Beata Anna; Oechslin, Erwin; Palmer, Lisa; Repetto, Gabriela M; Reyes, Nikolai Gil D; Schneider, Maude; Silversides, Candice; Sullivan, Kathleen E; Swillen, Ann; van Amelsvoort, Therese A M J; Van Batavia, Jason P; Vingerhoets, Claudia; McDonald-McGinn, Donna M; Bassett, Anne S.
Affiliation
  • Boot E; Advisium, 's Heeren Loo Zorggroep, Amersfoort, The Netherlands; The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada; Department of Psychiatry and Neuropsychology, Maastricht University, Maastricht, The Netherlands. Electronic address: erik.bo
  • Óskarsdóttir S; Department of Pediatric Rheumatology and Immunology, Queen Silvia Children's Hospital, Sahlgrenska University Hospital, Gothenburg, Sweden; Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. Electronic address: solveig.oskarsd
  • Loo JCY; The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.
  • Crowley TB; 22q and You Center, Clinical Genetics Center, and Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Orchanian-Cheff A; Library and Information Services, and The Institute of Education Research (TIER), University Health Network, Toronto, Ontario, Canada.
  • Andrade DM; Adult Genetic Epilepsy Program, Toronto Western Hospital and University of Toronto, Toronto, Ontario, Canada.
  • Arganbright JM; Division of Otolaryngology, Children's Mercy Hospital and University of Missouri Kansas City School of Medicine, Kansas City, MO.
  • Castelein RM; Department of Orthopedic Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Cserti-Gazdewich C; Hematology and Transfusion Medicine, University Health Network, Toronto, Ontario, Canada.
  • de Reuver S; Department of Orthopedic Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Fiksinski AM; Department of Psychiatry and Neuropsychology, Maastricht University, Maastricht, The Netherlands; Department of Pediatric Psychology, University Medical Centre, Wilhelmina Children's Hospital, Utrecht, The Netherlands.
  • Klingberg G; Faculty of Odontology, Malmö University, Malmö, Sweden.
  • Lang AE; The Edmond J. Safra Program in Parkinson's Disease and the Morton and Gloria Shulman Movement Disorders, Toronto Western Hospital, University Health Network, Toronto, Ontario, Canada.
  • Mascarenhas MR; Division of Gastroenterology and 22q and You Center, Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA.
  • Moss EM; Bryn Mawr, PA.
  • Nowakowska BA; Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland.
  • Oechslin E; Toronto Adult Congenital Heart Disease Program, Peter Munk Cardiac Centre, University Health Network and University of Toronto, Toronto, Ontario, Canada.
  • Palmer L; The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.
  • Repetto GM; Rare Diseases Program, Institute for Sciences and Innovation in Medicine, Facultad de Medicina Clinica Alemana Universidad del Desarrollo, Santiago, Chile.
  • Reyes NGD; The Edmond J. Safra Program in Parkinson's Disease and the Morton and Gloria Shulman Movement Disorders, Toronto Western Hospital, University Health Network, Toronto, Ontario, Canada.
  • Schneider M; Clinical Psychology Unit for Intellectual and Developmental Disabilities, Faculty of Psychology and Educational Sciences, University of Geneva, Geneva, Switzerland.
  • Silversides C; Toronto ACHD Program, Mount Sinai and Toronto General Hospitals, University of Toronto, Toronto, Ontario, Canada.
  • Sullivan KE; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA; Division of Allergy and Immunology and 22q and You Center, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Swillen A; Center for Human Genetics, University Hospital UZ Leuven, Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • van Amelsvoort TAMJ; Department of Psychiatry and Neuropsychology, Maastricht University, Maastricht, The Netherlands.
  • Van Batavia JP; Department of Surgery, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA; Division of Urology and 22q and You Center, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Vingerhoets C; Advisium, 's Heeren Loo Zorggroep, Amersfoort, The Netherlands; Department of Psychiatry and Neuropsychology, Maastricht University, Maastricht, The Netherlands.
  • McDonald-McGinn DM; 22q and You Center, Clinical Genetics Center, and Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA; Department of Human Biology and Medical Genetics, Sapienza U
  • Bassett AS; The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada; Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada; Clinical Genetics Research Program and Campbell Family Mental Health Research Institute, Centre for Addiction and
Genet Med ; 25(3): 100344, 2023 03.
Article in En | MEDLINE | ID: mdl-36729052
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DiGeorge Syndrome Type of study: Guideline / Prognostic_studies / Qualitative_research / Systematic_reviews Limits: Adult / Humans Language: En Journal: Genet Med Journal subject: GENETICA MEDICA Year: 2023 Document type: Article Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DiGeorge Syndrome Type of study: Guideline / Prognostic_studies / Qualitative_research / Systematic_reviews Limits: Adult / Humans Language: En Journal: Genet Med Journal subject: GENETICA MEDICA Year: 2023 Document type: Article Country of publication: