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Results for
""DiGeorge Syndrome""[mesh_terms]

20 Results

Searching titles within these results

Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.

Kathleen E Sullivan

Immunology and allergy clinics of North America 2008;28(2):353-66

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Abstract

Atypical microdeletion in 22q11 deletion syndrome reveals new candidate causative genes: A case report and literature review.

Huiping Shi, Zhaoyue Wang

Medicine 2018;97(8):e9936

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Abstract

Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome.

Sólveig Óskarsdóttir, Erik Boot, Terrence Blaine Crowley, Joanne C Y Loo, Jill M Arganbright, Marco Armando, Adriane L Baylis, Elemi J Breetvelt, René M Castelein, Madeline Chadehumbe, Christopher M Cielo, Steven de Reuver, Stephan Eliez, Ania M Fiksinski, Brian J Forbes, Emily Gallagher, Sarah E Hopkins, Oksana A Jackson, Lorraine Levitz-Katz, Gunilla Klingberg, Michele P Lambert, Bruno Marino, Maria R Mascarenhas, Julie Moldenhauer, Edward M Moss, Beata Anna Nowakowska, Ani Orchanian-Cheff, Carolina Putotto, Gabriela M Repetto, Erica Schindewolf, Maude Schneider, Cynthia B Solot, Kathleen E Sullivan, Ann Swillen, Marta Unolt, Jason P Van Batavia, Claudia Vingerhoets, Jacob Vorstman, Anne S Bassett, Donna M McDonald-McGinn

Genetics in medicine : official journal of the American College of Medical Genetics 2023;25(3):100338

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Late diagnosis of DiGeorge syndrome in a 13-year-old male with subclinical course of the disease - case report and literature review.

Aleksandra Janina Wylazłowska, Małgorzata Grabarczyk, Marta Gorczyca, Paweł Matusik

Pediatric endocrinology, diabetes, and metabolism 2024;29(4):259-266

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Effectiveness and side effects of psychopharmacotherapy in individuals with 22q11.2 deletion syndrome with comorbid psychiatric disorders: a systematic review.

Mariela Mosheva, Liran Korotkin, Raquel E Gur, Abraham Weizman, Doron Gothelf

European child & adolescent psychiatry 2020;29(8):1035-1048

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Orthopedic and orthodontic management in a patient with DiGeorge Syndrome and Familial Mediterranean Fever: A case report.

Angela Pia Cazzolla, Maria Grazia Lacaita, Vitantonio Lacarbonara, Khrystyna Zhurakivska, Annarosa De Franco, Irene Gissi, Nunzio Francesco Testa, Giuseppe Marzo, Lorenzo Lo Muzio

Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry 2019;39(3):340-347

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Long-term tolerance to allogeneic thymus transplants in complete DiGeorge anomaly.

Ivan K Chinn, Blythe H Devlin, Yi-Ju Li, M Louise Markert

Clinical immunology (Orlando, Fla.) 2008;126(3):277-81

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Cross-sectional and longitudinal findings in patients with proximal 22q11.2 duplication: A retrospective chart study.

Jente Verbesselt, Inge Zink, Jeroen Breckpot, Ann Swillen

American journal of medical genetics. Part A 2022;188(1):46-57

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Postnatal thymus transplantation with immunosuppression as treatment for DiGeorge syndrome.

M Louise Markert, Marilyn J Alexieff, Jie Li, Marcella Sarzotti, Daniel A Ozaki, Blythe H Devlin, Debra A Sedlak, Gregory D Sempowski, Laura P Hale, Henry E Rice, Samuel M Mahaffey, Michael A Skinner

Blood 2004;104(8):2574-81

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Outcomes of primary repair of cleft palate using sommerled intravelar veloplasty associated with velocardiofacial syndrome.

Parisa Rezaei, Awat Feizi, Sarah Esmailzade Moghimi, Saba Sadeghi, Fatemeh Derakhshandeh

International journal of pediatric otorhinolaryngology 2024;179():111940

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Vitamin D status and the immune assessment in 22q11.2 deletion syndrome.

A Legitimo, V Bertini, G Costagliola, G I Baroncelli, R Morganti, A Valetto, R Consolini

Clinical and experimental immunology 2020;200(3):272-286

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A practical approach to hypocalcaemia in children.

Nick Shaw

Endocrine development 2010;16():73-92

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Seizures and EEG findings in an adult patient with DiGeorge syndrome: a case report and review of the literature.

Walter González, Ramon Edmundo D Bautista

Seizure 2009;18(9):648-51

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Cinacalcet Treatment in an Adolescent With Concurrent 22q11.2 Deletion Syndrome and Familial Hypocalciuric Hypercalcemia Type 3 Caused by AP2S1 Mutation.

Sirpa Tenhola, Geoffrey N Hendy, Helena Valta, Lucie Canaff, Bonnie S P Lee, Betty Y L Wong, Matti J Välimäki, David E C Cole, Outi Mäkitie

The Journal of clinical endocrinology and metabolism 2015;100(7):2515-8

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Indicated prevention with long-chain polyunsaturated omega-3 fatty acids in patients with 22q11DS genetically at high risk for psychosis. Protocol of a randomized, double-blind, placebo-controlled treatment trial.

Marco Armando, Franco De Crescenzo, Stefano Vicari, Maria Cristina Digilio, Maria Pontillo, Francesco Papaleo, G Paul Amminger

Early intervention in psychiatry 2017;10(5):390-6

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Results: 1 – 15 / 20

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Results for ""DiGeorge Syndrome""[mesh_terms]

Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.

Atypical microdeletion in 22q11 deletion syndrome reveals new candidate causative genes: A case report and literature review.

Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome.

Late diagnosis of DiGeorge syndrome in a 13-year-old male with subclinical course of the disease - case report and literature review.

Effectiveness and side effects of psychopharmacotherapy in individuals with 22q11.2 deletion syndrome with comorbid psychiatric disorders: a systematic review.

Orthopedic and orthodontic management in a patient with DiGeorge Syndrome and Familial Mediterranean Fever: A case report.

Long-term tolerance to allogeneic thymus transplants in complete DiGeorge anomaly.

Cross-sectional and longitudinal findings in patients with proximal 22q11.2 duplication: A retrospective chart study.

Postnatal thymus transplantation with immunosuppression as treatment for DiGeorge syndrome.

Outcomes of primary repair of cleft palate using sommerled intravelar veloplasty associated with velocardiofacial syndrome.

Vitamin D status and the immune assessment in 22q11.2 deletion syndrome.

A practical approach to hypocalcaemia in children.

Seizures and EEG findings in an adult patient with DiGeorge syndrome: a case report and review of the literature.

Cinacalcet Treatment in an Adolescent With Concurrent 22q11.2 Deletion Syndrome and Familial Hypocalciuric Hypercalcemia Type 3 Caused by AP2S1 Mutation.

Indicated prevention with long-chain polyunsaturated omega-3 fatty acids in patients with 22q11DS genetically at high risk for psychosis. Protocol of a randomized, double-blind, placebo-controlled treatment trial.

Results for
""DiGeorge Syndrome""[mesh_terms]