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Bone Reports
|
March 13, 2023
<i>FLNA-</i>filaminopathy skeletal phenotypes are not due to an osteoblast autonomous loss-of-function
Emma M Wade, Elizabeth A Goodin, Yongqiang Wang, et al.
Revista Da Associacao Medica Brasileira (1992)
|
November 26, 2015
Menkes disease: importance of diagnosis with molecular analysis in the neonatal period
Larissa Sampaio de Athayde Costa, Stephanie Pucci Pegler, Rute Facchini Lellis, et al.
Physiology & Behavior
|
November 14, 2019
Mental health, stress, and resilience correlates of heart rate variability among military reservists, guardsmen, and first responders
Laurel L Hourani, Maria I Davila, Jessica Morgan, et al.
American Journal of Medical Genetics. Part A
|
July 9, 2011
Further expansion of the phenotypic spectrum associated with mutations in ALDH18A1, encoding Δ¹-pyrroline-5-carboxylate synthase (P5CS)
David L Skidmore, David Chitayat, Tim Morgan, et al.
American Journal of Medical Genetics. Part A
|
August 14, 2008
Spondyloepiphyseal dysplasia, Omani type: further definition of the phenotype
Mirjam H H van Roij, Shuji Mizumoto, Shuhei Yamada, et al.
Military Medicine
|
January 27, 2021
Use of Mobile Technology Paired with Heart Rate Monitor to Remotely Quantify Behavioral Health Markers among Military Reservists and First Responders
Maria I Davila, Paul N Kizakevich, Randy Eckhoff, et al.
Digestive Diseases and Sciences
|
January 18, 2007
Clinical implications of hepatic steatosis in patients with chronic hepatitis C: a multicenter study of U.S. veterans
Ke-Qin Hu, Sue L Currie, Hui Shen, et al.
American Journal of Human Genetics
|
March 31, 2015
Mutations in DVL1 cause an osteosclerotic form of Robinow syndrome
Kieran J Bunn, Phil Daniel, Heleen S Rösken, et al.
International Journal of Child Health and Nutrition
|
February 25, 2017
Comparing Two Waist-to-Height Ratio Measurements with Cardiometabolic Risk Factors among Youth with Diabetes
Lenna L Liu, Henry S Kahn, David J Pettitt, et al.
HGG Advances
|
March 14, 2026
Impaired retinoic acid receptor-γ signalling underlies a heritable form of urothelial keratinising squamous metaplasia
Kaya Fukushima, Nicole Avery, Jade Desjardins, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 45) with videos related to
Sort By:
Page
of 5
Bone Reports
|
March 13, 2023
<i>FLNA-</i>filaminopathy skeletal phenotypes are not due to an osteoblast autonomous loss-of-function
Emma M Wade, Elizabeth A Goodin, Yongqiang Wang, et al.
Revista Da Associacao Medica Brasileira (1992)
|
November 26, 2015
Menkes disease: importance of diagnosis with molecular analysis in the neonatal period
Larissa Sampaio de Athayde Costa, Stephanie Pucci Pegler, Rute Facchini Lellis, et al.
Physiology & Behavior
|
November 14, 2019
Mental health, stress, and resilience correlates of heart rate variability among military reservists, guardsmen, and first responders
Laurel L Hourani, Maria I Davila, Jessica Morgan, et al.
American Journal of Medical Genetics. Part A
|
July 9, 2011
Further expansion of the phenotypic spectrum associated with mutations in ALDH18A1, encoding Δ¹-pyrroline-5-carboxylate synthase (P5CS)
David L Skidmore, David Chitayat, Tim Morgan, et al.
American Journal of Medical Genetics. Part A
|
August 14, 2008
Spondyloepiphyseal dysplasia, Omani type: further definition of the phenotype
Mirjam H H van Roij, Shuji Mizumoto, Shuhei Yamada, et al.
Military Medicine
|
January 27, 2021
Use of Mobile Technology Paired with Heart Rate Monitor to Remotely Quantify Behavioral Health Markers among Military Reservists and First Responders
Maria I Davila, Paul N Kizakevich, Randy Eckhoff, et al.
Digestive Diseases and Sciences
|
January 18, 2007
Clinical implications of hepatic steatosis in patients with chronic hepatitis C: a multicenter study of U.S. veterans
Ke-Qin Hu, Sue L Currie, Hui Shen, et al.
American Journal of Human Genetics
|
March 31, 2015
Mutations in DVL1 cause an osteosclerotic form of Robinow syndrome
Kieran J Bunn, Phil Daniel, Heleen S Rösken, et al.
International Journal of Child Health and Nutrition
|
February 25, 2017
Comparing Two Waist-to-Height Ratio Measurements with Cardiometabolic Risk Factors among Youth with Diabetes
Lenna L Liu, Henry S Kahn, David J Pettitt, et al.
HGG Advances
|
March 14, 2026
Impaired retinoic acid receptor-γ signalling underlies a heritable form of urothelial keratinising squamous metaplasia
Kaya Fukushima, Nicole Avery, Jade Desjardins, et al.
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of 5