Sökresultat - Shashi, Vandana

Discordance in Diagnoses and Treatment of Psychiatric Disorders in Children and Adolescents with 22q11.2 Deletion Syndrome av Young, Andrea S., Shashi, Vandana, Schoch, Kelly, Kwapil, Thomas, Hooper, Stephen R.

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Assessment of Parental Disclosure of a 22q11.2 Deletion Syndrome Diagnosis and Implications for Clinicians av Faux, Dana, Schoch, Kelly, Eubanks, Sonja, Hooper, Stephen R., Shashi, Vandana

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A Longitudinal Examination of the Psychoeducational, Neurocognitive, and Psychiatric Functioning in Children with 22q11.2 Deletion Syndrome av Hooper, Stephen R., Curtiss, Kathleen, Schoch, Kelly, Keshavan, Matcheri S., Allen, Andrew, Shashi, Vandana

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A Unique Form of Mental Retardation with a Distinctive Phenotype Maps to Xq26-q27 av Shashi, Vandana, Berry, Margaret N., Shoaf, Sarah, Sciote, James J., Goldstein, Donald, Hart, Thomas C.

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Feasibility and Preliminary Efficacy Data from a Computerized Cognitive Intervention in Children with Chromosome 22q11.2 Deletion Syndrome av Harrell, Waverly, Eack, Shaun, Hooper, Stephen R., Keshavan, Matcheri S., Bonner, Melanie S., Schoch, Kelly, Shashi, Vandana

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PSEUDOMETABOLIC PRESENTATION OF DYSTROPHINOPATHY DUE TO A MISSENSE MUTATION av VEERAPANDIYAN, ARAVINDHAN, SHASHI, VANDANA, JIANG, YONG-HUI, GALLENTINE, WILLIAM BRIAN, SCHOCH, KELLY, SMITH, EDWARD CLINTON

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Frontal hypoactivation during a working memory task in children with 22q11 deletion syndrome av Harrell, Waverly, Zou, Ling, Englander, Zoe, Hooper, Stephen R., Keshavan, Matcheri S., Song, Allen, Shashi, Vandana

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Applicability of the Nonverbal Learning Disability Paradigm for Children With 22q11.2 Deletion Syndrome av Schoch, Kelly, Harrell, Waverly, Hooper, Stephen R., Ip, Edward H., Saldana, Santiago, Kwapil, Thomas R., Shashi, Vandana

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A tale worth telling: The impact of the diagnosis experience on disclosure of genetic disorders av Goodwin, Jane, Schoch, Kelly, Shashi, Vandana, Hooper, Stephen R., Gothelf, Doron, Zalevsky, Moran, Morad, Ola, Campbell, Linda E.

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Altered Development of the Dorsolateral Prefrontal Cortex in Chromosome 22q11.2 Deletion Syndrome: an in vivo (1)H Spectroscopy study av Shashi, Vandana, Veerapandiyan, Aravindhan, Keshavan, Matcheri S., Zapadka, Michael, Schoch, Kelly, Kwapil, Thomas R., Hooper, Stephen R., Stanley, Jeffrey A.

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COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome av Shashi, Vandana, Howard, Timothy D., Keshavan, Matcheri S., Kaczorowski, Jessica, Berry, Margaret N., Schoch, Kelly, Spence, Edward J., Kwapil, Thomas R.

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Socioeconomic Status and Psychological Function in Children with Chromosome 22q11.2 Deletion Syndrome: Implications for Genetic Counseling av Shashi, Vandana, Keshavan, Matcheri, Kaczorowski, Jessica, Schoch, Kelly, Lewandowski, Kathryn E., McConkie-Rosell, Allyn, Hooper, Stephen R., Kwapil, Thomas R.

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Clinical application of exome sequencing in undiagnosed genetic conditions av Need, Anna C, Shashi, Vandana, Hitomi, Yuki, Schoch, Kelly, Shianna, Kevin V, McDonald, Marie T, Meisler, Miriam H, Goldstein, David B

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Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms av Shashi, Vandana, Francis, Alan, Hooper, Stephen R, Kranz, Peter G, Zapadka, Michael, Schoch, Kelly, Ip, Edward, Tandon, Neeraj, Howard, Timothy D, Keshavan, Matcheri S

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A window into living with an undiagnosed disease: illness narratives from the Undiagnosed Diseases Network av Spillmann, Rebecca C., McConkie-Rosell, Allyn, Pena, Loren, Jiang, Yong-Hui, Schoch, Kelly, Walley, Nicole, Sanders, Camilla, Sullivan, Jennifer, Hooper, Stephen R., Shashi, Vandana

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Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing? av McConkie-Rosell, Allyn, Hooper, Stephen R., Pena, Loren D. M., Schoch, Kelly, Spillmann, Rebecca C., Jiang, Yong-Hui, Cope, Heidi, Palmer, Christina, Shashi, Vandana

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Clinical Application of a Scale to Assess Genomic Healthcare Empowerment (GEmS): Process and Illustrative Case Examples av McConkie-Rosell, Allyn, Schoch, Kelly, Sullivan, Jennifer, Spillmann, Rebecca C., Cope, Heidi, Tan, Queenie K.-G., Palmer, Christina G. S., Hooper, Stephen R., Shashi, Vandana

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Sustained therapeutic response to riboflavin in a child with a progressive neurological condition, diagnosed by whole-exome sequencing av Shashi, Vandana, Petrovski, Slavé, Schoch, Kelly, Crimian, Rebecca, Case, Laura E., Khalid, Roha, El-Dairi, Maysantoine A., Jiang, Yong-Hui, Mikati, Mohamad A., Goldstein, David B.

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Alternative transcripts in variant interpretation: the potential for missed diagnoses and misdiagnoses av Schoch, Kelly, Tan, Queenie K.-G., Stong, Nicholas, Deak, Kristen L., McConkie-Rosell, Allyn, McDonald, Marie T., Goldstein, David B., Jiang, Yong-hui, Shashi, Vandana

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Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome av Shashi, Vandana, Kwapil, Thomas R., Kaczorowski, Jessica, Berry, Margaret N., Santos, Cesar S., Howard, Timothy D., Goradia, Dhruman, Prasad, Konasale, Vaibhav, Diwadkar, Rajarethinam, Rajaprabhakaran, Spence, Edward, Keshavan, Matcheri S.

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