GMPPB-Associated Dystroglycanopathy: Emerging Common Variants with Phenotype Correlation von Jensen, Braden S., Willer, Tobias, Saade, Dimah N., Cox, Mary O., Mozaffar, Tahseen, Scavina, Mena, Stefans, Vikki A., Winder, Thomas L., Campbell, Kevin P., Moore, Steven A., Mathews, Katherine D.

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Poster 421 Primary Amoebic Meningitis Survivor Story from a Rehabilitation Point of View: A Case Report von Kamanga-Sollo, Gladys, MD, Tompkins, Esther H., DO, Stefans, Vikki A., MD

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Pulmonary embolism in rehabilitation patients: Relation to time before return to physical therapy after diagnosis of deep vein thrombosis von Kiser, Thomas S., Stefans, Vikki A.

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POSTER BOARD 101: RECOGNIZING SPINAL CORD TUMORS IN THE PEDIATRIC POPULATION von Foley, Regina P., Stefans, Vikki A., Williams, Sonia

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Poster 14 von Rao, Aruna D., Fann, Alice V., Stefans, Vikki A.

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Poster 14: Hypertension as the sole indication of posttraumatic hydrocephalus: a case report von Rao, Aruna D., Fann, Alice V., Stefans, Vikki A.

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Developing anxiety-reduction procedures for a ventilator-dependent pediatric patient von WARZAK, W. J, ENGEL, L. E, BISCHOFF, L. G, STEFANS, V. A

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Combination molecular therapies for type 1 spinal muscular atrophy von Harada, Yohei, Rao, Vamshi K., Arya, Kapil, Kuntz, Nancy L., DiDonato, Christine J., Napchan‐Pomerantz, Galia, Agarwal, Amit, Stefans, Vikki, Katsuno, Masahisa, Veerapandiyan, Aravindhan

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BAG3 Myopathy in Patient with Prominent Neuropathic Phenotype and no Cardiac or Respiratory Involvement (1420) von Malatesta, Lindsay, Veerapandiyan, Aravindhan, Arya, Kapil, Gokden, Murat, Stefans, Vikki

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Clinical and molecular spectrum of thymidine kinase 2-related mtDNA maintenance defect von Wang, Julia, Kim, Emily, Dai, Honzheng, Stefans, Vikki, Vogel, Hannes, Al Jasmi, Fatma, Schrier Vergano, Samantha A., Castro, Diana, Bernes, Saunder, Bhambhani, Vikas, Long, Catherine, El-Hattab, Ayman W., Wong, Lee-Jun

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Clinical Reasoning: A 6-Year-Old Boy With Muscle Twitching von Lewis, Hannah Smashey, Srinivasa Sekaran, Balaji Subramanian, Stefans, Vikki, Veerapandiyan, Aravindhan

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Anti-dopaminergic medication related myopathy causing respiratory muscle weakness without neuroleptic malignant syndrome (P3.461) von Harada, Yohei, Gokden, Murat, Virmani, Tuhin, Stefans, Vikki

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Combination therapy with nusinersen and AVXS-101: a real-world clinical experience (4152) von Harada, Yohei, Arya, Kapil, Napchan-Pomerantz, Galia, Kauffmann, Rondi, Agarwal, Amit, Stefans, Vikki, Veerapandiyan, Aravindhan

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Thrombotic Microangiopathy (TMA): A potential adverse reaction post Zolgensma (onasemnogene abeparvovec-xioi) therapy for Spinal Muscular Atrophy (SMA) (5483) von Prabhu, Nayana, Saylam, Ezgi, Louis, Cassandra, Moss, Michelle, Millner, Rachel, Douglass, David, Veerapandiyan, Aravindhan, Agarwal, Amit, Stefans, Vikki, Arya, Kapil

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Limb-Girdle Muscular Dystrophy R9 due to a Novel Complex Insertion/Duplication Variant in FKRP Gene von Willis, Erin, Moore, Steven A., Cox, Mary O., Stefans, Vikki, Aravindhan, Akilandeswari, Gokden, Murat, Veerapandiyan, Aravindhan

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Constitutive activation of the PI3K‐AKT pathway and cardiovascular abnormalities in an individual with Kosaki overgrowth syndrome von Zarate, Yuri A., Boccuto, Luigi, Srikanth, Sujata, Pauly, Rini, Ocal, Eylem, Balmakund, Tonya, Hinkle, Kevin, Stefans, Vikki, Schaefer, Gerald B., Collins, Ronnie Thomas

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De novo variants in EBF3 are associated with hypotonia, developmental delay, intellectual disability, and autism von Tanaka, Akemi J, Cho, Megan T, Willaert, Rebecca, Retterer, Kyle, Zarate, Yuri A, Bosanko, Katie, Stefans, Vikki, Oishi, Kimihiko, Williamson, Amy, Wilson, Golder N, Basinger, Alice, Barbaro-Dieber, Tina, Ortega, Lucia, Sorrentino, Susanna, Gabriel, Melissa K, Anderson, Ilse J, Sacoto, Maria J Guillen, Schnur, Rhonda E, Chung, Wendy K

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A novel noncoding FKRP mutation in early onset limb-girdle muscular dystrophy von Saylam, Ezgi, Moore, Steven A., Aravindhan, Akilandeswari, Marton, Heather, Nagy, Peter L., Gokden, Murat, Cox, Mary O., Stefans, Vikki, Veerapandiyan, Aravindhan

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Experiences from the development of a comprehensive family support program for pediatric trauma and rehabilitation patients von Aitken, Mary E., Korehbandi, Patricia, Parnell, Donna, Parker, James G., Stefans, Vikki, Tompkins, Esther, Schulz, Eldon G.

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Limb-Girdle Muscular Dystrophy R9 due to a Novel Complex Insertion/Duplication Variant in FKRP Gene von Willis, Erin, Moore, Steven A, Cox, Mary O, Stefans, Vikki, Aravindhan, Akilandeswari, Gokden, Murat, Veerapandiyan, Aravindhan

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