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Crenshaw, Melissa L.
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1

PURA syndrome: Neuromuscular junction manifestations with p..:

Iyadurai, Stanley ; Geller, Thomas ; Wyrebek, Rita...
Neuromuscular Disorders.  33 (2023)  8 - p. 699 , 2023
Link: https://doi.org/10.1016/..
 
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2

Response to Letter to the Editor:

Baldwin, Kelli ; Karjoo, Sara ; Crenshaw, Melissa
Clinical Pediatrics.  61 (2022)  8 - p. 587-587 , 2022
Link: https://doi.org/10.1177/..
 
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3

Hypotonic infant with PURA syndrome-related channelopathy s..:

Wyrebek, Rita ; DiBartolomeo, Mara ; Brooks, Sandra...
Neuromuscular Disorders.  32 (2022)  2 - p. 166-169 , 2022
Link: https://doi.org/10.1016/..
 
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4

Corrigendum to 'Hypotonic Infant with PURA Syndrome-related..:

Wyrebek, Rita ; Bartolomeo, Mara Di ; Brooks, Sandra...
Neuromuscular Disorders.  32 (2022)  8 - p. e1 , 2022
Link: https://doi.org/10.1016/..
 
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5

Novel KIAA1033/WASHC4 mutations in three patients with synd..:

Assoum, Mirna ; Bruel, Ange‐Line ; Crenshaw, Melissa L....
American Journal of Medical Genetics Part A.  182 (2020)  4 - p. 792-797 , 2020
Link: https://doi.org/10.1002/..
 
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6

"Donating our bodies to science": A discussion about autops..:

Prakash, Siddharth K. ; San Roman, Adrianna K. ; Crenshaw, Melissa...
American Journal of Medical Genetics Part C: Seminars in Medical Genetics.  181 (2019)  1 - p. 22-28 , 2019
Link: https://doi.org/10.1002/..
 
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7

The Turner syndrome research registry: Creating equipoise b..:

Prakash, Siddharth K. ; Lugo‐Ruiz, Soniely ; Rivera‐Dávila, Michelle...
American Journal of Medical Genetics Part C: Seminars in Medical Genetics.  181 (2019)  1 - p. 7-12 , 2019
Link: https://doi.org/10.1002/..
 
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8

45,X mosaicism in a population-based biobank: implications ..:

Prakash, Siddharth K. ; Crenshaw, Melissa L. ; Backeljauw, Philippe F....
Genetics in Medicine.  21 (2019)  8 - p. 1882-1883 , 2019
Link: https://doi.org/10.1038/..
 
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9

Recognition and management of adults with Turner syndrome: ..:

Lin, Angela E. ; Prakash, Siddharth K. ; Andersen, Niels H....
American Journal of Medical Genetics Part A.  179 (2019)  10 - p. 1987-2033 , 2019
Link: https://doi.org/10.1002/..
 
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10

B-cell acute lymphoblastic leukemia with high mutation burd..:

Oshrine, Benjamin ; Grana, Nanette ; Moore, Colin...
Blood Advances.  3 (2019)  12 - p. 1795-1798 , 2019
Link: https://doi.org/10.1182/..
 
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11

A patient with Phelan‐McDermid syndrome and dilation of the..:

Deibert, Emily ; Crenshaw, Melissa ; Miller, Michelle S.
Clinical Case Reports.  7 (2019)  4 - p. 607-611 , 2019
Link: https://doi.org/10.1002/..
 
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12

MBCL-46. COMPOUND HETEROZYGOUS MUTATION OF THE PMS2 GENE IN..:

Lukas, Claudia ; Crenshaw, Melissa ; Gonzalez-Gomez, Ignacio...
Neuro-Oncology.  20 (2018)  suppl_2 - p. i127-i127 , 2018
Link: https://doi.org/10.1093/..
 
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13

Genotype-Phenotype Correlation in NF1: Evidence for a More ..:

Koczkowska, Magdalena ; Chen, Yunjia ; Callens, Tom...
The American Journal of Human Genetics.  102 (2018)  1 - p. 69-87 , 2018
Link: https://doi.org/10.1016/..
 
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14

Proposal for a national registry to monitor women with Turn..:

Lin, Angela E. ; Karnis, Megan F. ; Calderwood, Laurel...
Fertility and Sterility.  105 (2016)  6 - p. 1446-1448 , 2016
Link: https://doi.org/10.1016/..
 
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15

High Incidence of Noonan Syndrome Features Including Short ..:

Rojnueangnit, Kitiwan ; Xie, Jing ; Gomes, Alicia...
Human Mutation.  36 (2015)  11 - p. 1052-1063 , 2015
Link: https://doi.org/10.1002/..
 
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