Search Results - "Kuensting, Timothy"

Prevalence and Impact of Underlying Diagnosis and Comorbidities on Chiari 1 Malformation by Sadler, Brooke, Kuensting, Timothy, Strahle, Jennifer, Park, Tae Sung, Smyth, Matthew, Limbrick, David D., Dobbs, Matthew B., Haller, Gabe, Gurnett, Christina A.

“…Chiari malformation type 1 affects approximately one in 1,000 people symptomatically, although one in 100 meet radiological criteria, making it a common…”
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Rare and de novo coding variants in chromodomain genes in Chiari I malformation by Sadler, Brooke, Wilborn, Jackson, Antunes, Lilian, Kuensting, Timothy, Hale, Andrew T., Gannon, Stephen R., McCall, Kevin, Cruchaga, Carlos, Harms, Matthew, Voisin, Norine, Reymond, Alexandre, Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Tartaglia, Marco, Niceta, Marcello, Leoni, Chiara, Zampino, Giuseppe, Ashley-Koch, Allison, Urbizu, Aintzane, Garrett, Melanie E., Soldano, Karen, Macaya, Alfons, Conrad, Donald, Strahle, Jennifer, Dobbs, Matthew B., Turner, Tychele N., Shannon, Chevis N., Brockmeyer, Douglas, Limbrick, David D., Gurnett, Christina A., Haller, Gabe

“…Chiari I malformation (CM1), the displacement of the cerebellum through the foramen magnum into the spinal canal, is one of the most common pediatric…”
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Obex position is associated with syringomyelia and use of posterior fossa decompression among patients with Chiari I malformation by Haller, Gabe, Sadler, Brooke, Kuensting, Timothy, Lakshman, Nivan, Greenberg, Jacob K, Strahle, Jennifer M, Park, Tae Sung, Dobbs, Matthew B, Gurnett, Christina A, Limbrick, David D

“…Chiari I malformation (CM-I) has traditionally been defined by measuring the position of the cerebellar tonsils relative to the foramen magnum. The…”
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Rare and de novo coding variants in chromodomain genes in Chiari I malformation by Sadler, Brooke, Wilborn, Jackson, Antunes, Lilian, Kuensting, Timothy, Hale, Andrew T., Gannon, Stephen R., McCall, Kevin, Cruchaga, Carlos, Harms, Matthew, Voisin, Norine, Reymond, Alexandre, Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Tartaglia, Marco, Niceta, Marcello, Leoni, Chiara, Zampino, Giuseppe, Ashley-Koch, Allison, Urbizu, Aintzane, Garrett, Melanie E., Soldano, Karen, Macaya, Alfons, Conrad, Donald, Strahle, Jennifer, Dobbs, Matthew B., Turner, Tychele N., Shannon, Chevis N., Brockmeyer, Douglas, Limbrick, David D., Gurnett, Christina A., Haller, Gabe

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Rare and de novo coding variants in chromodomain genes in Chiari I malformation by Sadler, Brooke, Wilborn, Jackson, Antunes, Lilian, Kuensting, Timothy, Hale, Andrew T., Gannon, Stephen R., McCall, Kevin, Cruchaga, Carlos, Harms, Matthew, Voisin, Norine, Reymond, Alexandre, Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Tartaglia, Marco, Niceta, Marcello, Leoni, Chiara, Zampino, Giuseppe, Ashley-Koch, Allison, Urbizu, Aintzane, Garrett, Melanie E., Soldano, Karen, Macaya, Alfons, Conrad, Donald, Strahle, Jennifer, Dobbs, Matthew B., Turner, Tychele N., Shannon, Chevis N., Brockmeyer, Douglas, Limbrick, David D., Gurnett, Christina A., Haller, Gabe

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Lack of joint hypermobility increases the risk of surgery in adolescent idiopathic scoliosis by Haller, Gabe, Zabriskie, Hannah, Spehar, Shelby, Kuensting, Timothy, Bledsoe, Xavier, Syed, Ali, Gurnett, Christina A, Dobbs, Matthew B

“…Generalized joint hypermobility (GJH) is a risk factor for developing adolescent idiopathic scoliosis (AIS); however, it is not known whether joint…”
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