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Hans Andersson, MD
Hans Andersson, MD
Hayward Genetics Center, Tulane University School of Medicine
Verified email at tulane.edu
Title
Cited by
Cited by
Year
Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: a report from the Gaucher Registry
NJ Weinreb, J Charrow, HC Andersson, P Kaplan, EH Kolodny, P Mistry, ...
The American journal of medicine 113 (2), 112-119, 2002
7072002
The Gaucher registry: demographics and disease characteristics of 1698 patients with Gaucher disease
J Charrow, HC Andersson, P Kaplan, EH Kolodny, P Mistry, G Pastores, ...
Archives of internal medicine 160 (18), 2835-2843, 2000
6452000
Phenylalanine hydroxylase deficiency: diagnosis and management guideline
J Vockley, HC Andersson, KM Antshel, NE Braverman, BK Burton, ...
Genetics in medicine 16 (2), 188-200, 2014
6242014
Mutations in the 3β-hydroxysterol Δ24-reductase gene cause desmosterolosis, an autosomal recessive disorder of cholesterol biosynthesis
HR Waterham, J Koster, GJ Romeijn, RCM Hennekam, P Vreken, ...
The American Journal of Human Genetics 69 (4), 685-694, 2001
3922001
The clinical and demographic characteristics of nonneuronopathic Gaucher disease in 887 children at diagnosis
P Kaplan, HC Andersson, KA Kacena, JD Yee
Archives of pediatrics & adolescent medicine 160 (6), 603-608, 2006
2712006
Gaucher disease type 1: revised recommendations on evaluations and monitoring for adult patients
NJ Weinreb, MC Aggio, HC Andersson, G Andria, J Charrow, JTR Clarke, ...
Seminars in hematology 41, 15-22, 2004
2122004
Eight-year clinical outcomes of long-term enzyme replacement therapy for 884 children with Gaucher disease type 1
H Andersson, P Kaplan, K Kacena, J Yee
Pediatrics 122 (6), 1182-1190, 2008
2062008
Enzyme replacement therapy and monitoring for children with type 1 Gaucher disease: consensus recommendations
J Charrow, HC Andersson, P Kaplan, EH Kolodny, P Mistry, G Pastores, ...
The Journal of pediatrics 144 (1), 112-120, 2004
2062004
Individualization of long-term enzyme replacement therapy for Gaucher disease
HC Andersson, J Charrow, P Kaplan, P Mistry, GM Pastores, ...
Genetics in Medicine 7 (2), 105-110, 2005
1832005
Desmosterolosis presenting with multiple congenital anomalies and profound developmental delay
HC Andersson, L Kratz, R Kelley
American journal of medical genetics 113 (4), 315-319, 2002
1312002
American College of Medical Genetics and Genomics Therapeutics Committee. Phenylalanine hydroxylase deficiency: diagnosis and management guideline
J Vockley, HC Andersson, KM Antshel, NE Braverman, BK Burton, ...
Genet Med 16 (2), 188-200, 2014
1102014
Biochemical and clinical response to hydroxocobalamin versus cyanocobalamin treatment in patients with methylmalonic acidemia and homocystinuria (cblC)
HC Andersson, E Shapira
The Journal of pediatrics 132 (1), 121-124, 1998
981998
The 2019 US medical genetics workforce: a focus on clinical genetics
BD Jenkins, CG Fischer, CA Polito, DR Maiese, AS Keehn, M Lyon, ...
Genetics in Medicine 23 (8), 1458-1464, 2021
892021
Swallowing dysfunction in nephropathic cystinosis
BC Sonies, EF Ekman, HC Andersson, MD Adamson, SG Kaler, ...
New England Journal of Medicine 323 (9), 565-570, 1990
891990
Long-term outcome in treated combined methylmalonic acidemia and homocystinemia
HC Andersson, M Marble, E Shapira
Genetics in Medicine 1 (4), 146-150, 1999
781999
Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical cases
B Xiang, H Zhu, Y Shen, DT Miller, K Lu, X Hu, HC Andersson, ...
The Journal of Molecular Diagnostics 12 (2), 204-212, 2010
772010
Adrenal insufficiency in Smith‐Lemli‐Opitz syndrome
HC Andersson, J Frentz, JE Martínez, CM Tuck‐Muller, J Bellizaire
American journal of medical genetics 82 (5), 382-384, 1999
711999
Autism in patients with propionic acidemia
P Witters, E Debbold, K Crivelly, KV Kerckhove, K Corthouts, B Debbold, ...
Molecular genetics and metabolism 119 (4), 317-321, 2016
672016
FGF21 underlies a hormetic response to metabolic stress in methylmalonic acidemia
I Manoli, JR Sysol, MW Epping, L Li, C Wang, JL Sloan, A Pass, J Gagné, ...
JCI insight 3 (23), 2018
562018
Clinical application of microarray-based molecular cytogenetics: an emerging new era of genomic medicine
MM Li, HC Andersson
The Journal of pediatrics 155 (3), 311-317, 2009
522009
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