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Current Opinion in Lipidology
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August 8, 2014
Sortilin and lipoprotein metabolism: making sense out of complexity
Alanna Strong, Kevin Patel, Daniel J Rader
Orphanet Journal of Rare Diseases
|
February 26, 2020
Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency
Amanda Barone Pritchard, Alanna Strong, Can Ficicioglu
American Journal of Medical Genetics. Part A
|
February 6, 2021
A novel heterotaxy gene: Expansion of the phenotype of TTC21B-spectrum disease
Alanna Strong, Dong Li, Frank Mentch, et al.
Clinical Liver Disease
|
November 8, 2021
Hepatic Manifestations of Urea Cycle Disorders
Alanna Strong, Jessica Gold, Nina B Gold, et al.
American Journal of Medical Genetics. Part A
|
April 1, 2025
A New EP300-Related Syndrome With Prominent Developmental and Immune Phenotypes
Devi Priyanka Maripuri, Jessica Gold, Nina Gold, et al.
American Journal of Medical Genetics. Part A
|
February 5, 2026
Novel Features of RASopathies: Liver Disease as an Emerging Phenotype
Alyssa L Rippert, Alanna Strong, Rebecca C Ahrens-Nicklas
Journal of Inherited Metabolic Disease
|
September 30, 2025
Are Inherited Metabolic Disorders More Common and Less Predictable Than We Thought?
Nina B Gold, Alanna Strong, Harini Somanchi, et al.
Ophthalmic Genetics
|
January 4, 2021
Ocular manifestations and surgical interventions in pediatric patients with Koolen-de-Vries syndrome
Daphna Prat, William R Katowitz, Alanna Strong, et al.
American Journal of Medical Genetics. Part A
|
March 26, 2018
Isosorbide dinitrate in nephronophthisis treatment
Alanna Strong, Samina Muneeruddin, Richard Parrish, et al.
Orphanet Journal of Rare Diseases
|
May 2, 2021
Ocular manifestations of ectodermal dysplasia
Daphna Landau Prat, William R Katowitz, Alanna Strong, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 69) with videos related to
Sort By:
Page
of 7
Current Opinion in Lipidology
|
August 8, 2014
Sortilin and lipoprotein metabolism: making sense out of complexity
Alanna Strong, Kevin Patel, Daniel J Rader
Orphanet Journal of Rare Diseases
|
February 26, 2020
Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency
Amanda Barone Pritchard, Alanna Strong, Can Ficicioglu
American Journal of Medical Genetics. Part A
|
February 6, 2021
A novel heterotaxy gene: Expansion of the phenotype of TTC21B-spectrum disease
Alanna Strong, Dong Li, Frank Mentch, et al.
Clinical Liver Disease
|
November 8, 2021
Hepatic Manifestations of Urea Cycle Disorders
Alanna Strong, Jessica Gold, Nina B Gold, et al.
American Journal of Medical Genetics. Part A
|
April 1, 2025
A New EP300-Related Syndrome With Prominent Developmental and Immune Phenotypes
Devi Priyanka Maripuri, Jessica Gold, Nina Gold, et al.
American Journal of Medical Genetics. Part A
|
February 5, 2026
Novel Features of RASopathies: Liver Disease as an Emerging Phenotype
Alyssa L Rippert, Alanna Strong, Rebecca C Ahrens-Nicklas
Journal of Inherited Metabolic Disease
|
September 30, 2025
Are Inherited Metabolic Disorders More Common and Less Predictable Than We Thought?
Nina B Gold, Alanna Strong, Harini Somanchi, et al.
Ophthalmic Genetics
|
January 4, 2021
Ocular manifestations and surgical interventions in pediatric patients with Koolen-de-Vries syndrome
Daphna Prat, William R Katowitz, Alanna Strong, et al.
American Journal of Medical Genetics. Part A
|
March 26, 2018
Isosorbide dinitrate in nephronophthisis treatment
Alanna Strong, Samina Muneeruddin, Richard Parrish, et al.
Orphanet Journal of Rare Diseases
|
May 2, 2021
Ocular manifestations of ectodermal dysplasia
Daphna Landau Prat, William R Katowitz, Alanna Strong, et al.
Page
of 7