Search Results - "Melvin, Pamela"

Phenotypic Variability of Osteogenesis Imperfecta Type V Caused by an IFITM5 Mutation by Shapiro, Jay R, Lietman, Caressa, Grover, Monica, Lu, James T, Nagamani, Sandesh CS, Dawson, Brian C, Baldridge, Dustin M, Bainbridge, Matthew N, Cohn, Dan H, Blazo, Maria, Roberts, Timothy T, Brennen, Feng‐Shu, Wu, Yimei, Gibbs, Richard A, Melvin, Pamela, Campeau, Philippe M, Lee, Brendan H

“…ABSTRACT In a large cohort of osteogenesis imperfecta type V (OI type V) patients (17 individuals from 12 families), we identified the same mutation in the 5′…”
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(3) Day-Night Activity Rhythms in Children Admitted to the Pediatric ICU for Non-Surgical Diagnoses by Kudchadkar, Sapna R., Alsafi, Eman, Melvin, Pamela

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Cross-sectional and longitudinal growth patterns in osteogenesis imperfecta: implications for clinical care by Germain-Lee, Emily L., Brennen, Feng-Shu, Stern, Diana, Kantipuly, Aditi, Melvin, Pamela, Terkowitz, Mia S., Shapiro, Jay R.

“…Background: There is strikingly limited information on linear growth and weight in the different types of osteogenesis imperfecta (OI). Here, we define growth…”
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Focus on function: Therapies for adults with attention-deficit/hyperactivity disorder by Sater, Pamela Ann Melvin

“…Attention-deficit/hyperactivity disorder (ADHD) is a common disorder affecting people of all ages, and is characterized by inattention, hyperactivity, and…”
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Focus on function by Sater Pamela Ann Melvin

“…Attention-deficit/hyperactivity disorder (ADHD) is a common disorder affecting people of all ages, and is characterized by inattention, hyperactivity, and…”
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Phenotypic Variability of Osteogenesis Imperfecta Type V Caused by an IFITM 5 Mutation by Shapiro, Jay R, Lietman, Caressa, Grover, Monica, Lu, James T, Nagamani, Sandesh CS, Dawson, Brian C, Baldridge, Dustin M, Bainbridge, Matthew N, Cohn, Dan H, Blazo, Maria, Roberts, Timothy T, Brennen, Feng-Shu, Wu, Yimei, Gibbs, Richard A, Melvin, Pamela, Campeau, Philippe M, Lee, Brendan H

“…ABSTRACT   In a large cohort of osteogenesis imperfecta type V (OI type V) patients (17 individuals from 12 families), we identified the same mutation in the…”
Get full text