Ngā hua rapu - Viskochil, David H. 

It takes two to tango: mast cell and Schwann cell interactions in neurofibromas mā Viskochil, David H.

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Clinical and Molecular Aspects of an Informative Family with Neurofibromatosis Type 1 and Noonan Phenotype mā Stevenson, David A., Viskochil, David H., Rope, Alan F., Carey, John C.

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NF1 Exon 22 Analysis of Individuals with the Clinical Diagnosis of Neurofibromatosis Type 1 mā Muram-Zborovski, Talia M., Vaughn, Cecily P., Viskochil, David H., Hanson, Heather, Mao, Rong, Stevenson, David A.

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Motor Proficiency in Children with Neurofibromatosis Type 1 mā Johnson, Barbara, MacWilliams, Bruce, Carey, John C., Viskochil, David H., D’Astous, Jacques L., Stevenson, David A.

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SPRED1 Mutations in a Neurofibromatosis Clinic mā Muram-Zborovski, Talia M, Stevenson, David A, Viskochil, David H, Dries, David C, Wilson, Andrew R, Mao, Rong

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Lower Extremity Strength and Hopping and Jumping Ground Reaction forces in Children with Neurofibromatosis Type 1 mā Johnson, Barbara, MacWilliams, Bruce, Carey, John C., Viskochil, David H., D’Astous, Jacques L., Stevenson, David A.

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Bone Mineral Density in Children and Adolescents with Neurofibromatosis Type 1 mā Stevenson, David A., Moyer-Mileur, Laurie J., Murray, Mary, Slater, Hillarie, Sheng, Xiaoming, Carey, John C., Dube, Bukhosi, Viskochil, David H.

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Racial/ethnic disparities and incidence of malignant peripheral nerve sheath tumors: results from the Surveillance, Epidemiology, and End Results program, 2000–2014 mā Peckham-Gregory, Erin C., Montenegro, Roberto E., Stevenson, David A., Viskochil, David H., Scheurer, Michael E., Lupo, Philip J., Schiffman, Joshua D.

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Evaluation of racial disparities in pediatric optic pathway glioma incidence: results from the Surveillance, Epidemiology, and End Results program, 2000–2014 mā Peckham-Gregory, Erin C., Montenegro, Roberto E., Stevenson, David A., Viskochil, David H., Scheurer, Michael E., Lupo, Philip J., Schiffman, Joshua D.

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Double Inactivation of NF1 in Tibial Pseudarthrosis mā Stevenson, David A., Zhou, Holly, Ashrafi, Shadi, Messiaen, Ludwine M., Carey, John C., D’Astous, Jacques L., Santora, Stephen D., Viskochil, David H.

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Analysis of Radiographic Characteristics of Anterolateral Bowing of the Lower Leg Prior to Fracture in Neurofibromatosis Type 1 mā Stevenson, David A., Carey, John C., Viskochil, David H., Moyer-Mileur, Laurie J., Slater, Hillarie, Murray, Mary A., D’Astous, Jacques L., Murray, Kathleen A.

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Tibial Geometry in Individuals with Neurofibromatosis Type 1 without Anterolateral Bowing of the Lower Leg Using Peripheral Quantitative Computed Tomography mā Stevenson, David A., Viskochil, David H., Carey, John C., Slater, Hillarie, Murray, Mary, Sheng, Xiaoming, D’Astous, Jacques, Hanson, Heather, Schorry, Elizabeth, Moyer-Mileur, Laurie J.

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The Use of Anterolateral Bowing of the Lower Leg in the Diagnostic Criteria for Neurofibromatosis Type 1 mā Stevenson, David A., Viskochil, David H., Schorry, Elizabeth K., Crawford, Alvin H., D’Astous, Jacques, Murray, Kathleen A., Friedman, J. M., Armstrong, Linlea, Carey, John C.

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Evidence of Increased Bone Resorption in Neurofibromatosis Type 1 Using Urinary Pyridinium Crosslink Analysis mā STEVENSON, DAVID A., SCHWARZ, ELISABETH L., VISKOCHIL, DAVID H., MOYER-MILEUR, LAURIE J., MURRAY, MARY, FIRTH, SEAN D., D’ASTOUS, JACQUES L., CAREY, JOHN C., PASQUALI, MARZIA

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A Novel Mutation in FGFR3 Causes Camptodactyly, Tall Stature, and Hearing Loss (CATSHL) Syndrome mā Toydemir, Reha M., Brassington, Anna E., Bayrak-Toydemir, Pınar, Krakowiak, Patrycja A., Jorde, Lynn B., Whitby, Frank G., Longo, Nicola, Viskochil, David H., Carey, John C., Bamshad, Michael J.

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Costello and Cardio-Facio-Cutaneous Syndromes: Moving Toward Clinical Trials in RASopathies mā RAUEN, KATHERINE A., BANERJEE, ANURADHA, BISHOP, W. ROBERT, LAUCHLE, JENNIFER O., MCCORMICK, FRANK, MCMAHON, MARTIN, MELESE, TERI, MUNSTER, PAMELA N., NADAF, SORENA, PACKER, ROGER J., SEBOLT-LEOPOLD, JUDITH, VISKOCHIL, DAVID H.

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Pediatric 25-Hydroxyvitamin D Concentrations in Neurofibromatosis Type 1 mā Stevenson, David A., Viskochil, David H., Carey, John C., Sheng, Xiaoming, Murray, Mary, Moyer-Mileur, Laurie, Shelton, Judd, Roberts, William L., Bunker, Ashley M., Hanson, Heather, Bauer, Stephanie, D’Astous, Jacques L.

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An Attenuated Phenotype of Costello Syndrome in Three Unrelated Individuals with a HRAS c.179G>A (p.Gly60Asp) Correlates with Uncommon Functional Consequences mā Gripp, Karen W., Sol-Church, Katia, Smpokou, Patroula, Graham, Gail E., Stevenson, David A., Hanson, Heather, Viskochil, David H., Baker, Laura C., Russo, Bridget, Gardner, Nick, Stabley, Deborah L., Kolbe, Verena, Rosenberger, Georg

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Bone Resorption in Syndromes of the Ras/MAPK Pathway mā Stevenson, David A., Schwarz, E.L., Carey, John C., Viskochil, David H., Hanson, Heather, Bauer, Stephanie, Weng, Hsin-Yi Cindy, Greene, Tom, Reinker, Kent, Swensen, Jeffrey, Chan, Rebecca J., Yang, Feng-Chun, Senbanjo, Linda, Yang, Zhenyun, Mao, Rong, Pasquali, Marzia

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Neurofibromin Deficiency-Associated Transcriptional Dysregulation Suggests a Novel Therapy for Tibial Pseudoarthrosis in NF1 mā Paria, Nandina, Cho, Tae-Joon, Choi, In Ho, Kamiya, Nobuhiro, Kayembe, Kay, Mao, Rong, Margraf, Rebecca L., Obermosser, Gerlinde, Oxendine, Ila, Sant, David W., Song, Mi Hyun, Stevenson, David A., Viskochil, David H., Wise, Carol A., Kim, Harry K.W., Rios, Jonathan J

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