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Cold Spring Harbor Symposia on Quantitative Biology
|
March 27, 2007
Small RNA regulators and the bacterial response to stress
S Gottesman, C A McCullen, M Guillier, et al.
Clinical Case Reports
|
June 8, 2017
Acromelia-oligodontia syndrome
Jyothirmai Talasila, Ramaswamy Pachigolla, Kiranmai V S N Yarlagadda, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 6, 2021
Health Care Transition From Pediatric- to Adult-Focused Care in X-linked Hypophosphatemia: Expert Consensus
Kathryn Dahir, Ruban Dhaliwal, Jill Simmons, et al.
Bone
|
May 16, 2019
New explanation for autosomal dominant high bone mass: Mutation of low-density lipoprotein receptor-related protein 6
Michael P Whyte, William H McAlister, Fan Zhang, et al.
American Journal of Medical Genetics. Part A
|
November 9, 2011
Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A
Fuki M Hisama, Davor Lessel, Dru Leistritz, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 23, 2018
Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1,25-Dihydroxyvitamin D-Mediated Hypercalcemia and Generalized Osteosclerosis
Michael P Whyte, Emilina Lim, William H McAlister, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
September 14, 2012
Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancy
Jesse E Otero, Gary S Gottesman, William H McAlister, et al.
Bone
|
July 31, 2024
Transmembrane protein 53 craniotubular dysplasia (OMIM # 619727): The skeletal disease and consequent blindness of this new disorder
Michael P Whyte, Robert S Weinstein, Paul H Phillips, et al.
NEJM Evidence
|
May 21, 2024
Broadening Eligibility Criteria and Diversity among Patients for Cancer Clinical Trials
Maneet Kaur, Filip Frahm, Yichen Lu, et al.
Bone
|
April 17, 2020
Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7)
Michael P Whyte, Philippe M Campeau, William H McAlister, et al.
Page
of 17
Search research articles
Search
Showing results (141-150 of 168) with videos related to
Sort By:
Page
of 17
Cold Spring Harbor Symposia on Quantitative Biology
|
March 27, 2007
Small RNA regulators and the bacterial response to stress
S Gottesman, C A McCullen, M Guillier, et al.
Clinical Case Reports
|
June 8, 2017
Acromelia-oligodontia syndrome
Jyothirmai Talasila, Ramaswamy Pachigolla, Kiranmai V S N Yarlagadda, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 6, 2021
Health Care Transition From Pediatric- to Adult-Focused Care in X-linked Hypophosphatemia: Expert Consensus
Kathryn Dahir, Ruban Dhaliwal, Jill Simmons, et al.
Bone
|
May 16, 2019
New explanation for autosomal dominant high bone mass: Mutation of low-density lipoprotein receptor-related protein 6
Michael P Whyte, William H McAlister, Fan Zhang, et al.
American Journal of Medical Genetics. Part A
|
November 9, 2011
Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A
Fuki M Hisama, Davor Lessel, Dru Leistritz, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 23, 2018
Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1,25-Dihydroxyvitamin D-Mediated Hypercalcemia and Generalized Osteosclerosis
Michael P Whyte, Emilina Lim, William H McAlister, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
September 14, 2012
Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancy
Jesse E Otero, Gary S Gottesman, William H McAlister, et al.
Bone
|
July 31, 2024
Transmembrane protein 53 craniotubular dysplasia (OMIM # 619727): The skeletal disease and consequent blindness of this new disorder
Michael P Whyte, Robert S Weinstein, Paul H Phillips, et al.
NEJM Evidence
|
May 21, 2024
Broadening Eligibility Criteria and Diversity among Patients for Cancer Clinical Trials
Maneet Kaur, Filip Frahm, Yichen Lu, et al.
Bone
|
April 17, 2020
Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7)
Michael P Whyte, Philippe M Campeau, William H McAlister, et al.
Page
of 17