The phenotype and genotype of mevalonate kinase deficiency: a series of 114 cases from the Eurofever registry
NM Ter Haar, J Jeyaratnam… - Arthritis & …, 2016 - Wiley Online Library
Objective Mevalonate kinase deficiency (MKD) is a rare metabolic disease characterized by
recurrent inflammatory episodes. This study was undertaken to describe the genotype …
recurrent inflammatory episodes. This study was undertaken to describe the genotype …
The phenotype and genotype of mevalonate kinase deficiency: a series of 114 cases from the Eurofever Registry
J Jeyaratnam, A Simon, P Brogan… - ARTHRITIS & …, 2016 - publicatt.unicatt.it
OBJECTIVE: Mevalonate kinase deficiency (MKD) is a rare metabolic disease characterized
by recurrent inflammatory episodes. This study was undertaken to describe the genotype …
by recurrent inflammatory episodes. This study was undertaken to describe the genotype …
The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From the Eurofever Registry.
NM Ter Haar, J Jeyaratnam, HJ Lachmann… - Arthritis & …, 2016 - europepmc.org
Objective Mevalonate kinase deficiency (MKD) is a rare metabolic disease characterized by
recurrent inflammatory episodes. This study was undertaken to describe the genotype …
recurrent inflammatory episodes. This study was undertaken to describe the genotype …
The phenotype and genotype of mevalonate kinase deficiency: a series of 114 cases from the Eurofever Registry
NM Ter Haar, J Jeyaratnam, HJ Lachmann… - Arthritis & …, 2016 - discovery.ucl.ac.uk
OBJECTIVES: Mevalonate kinase deficiency (MKD) is a rare metabolic disease
characterized by recurrent inflammatory episodes. This study aimed to describe the …
characterized by recurrent inflammatory episodes. This study aimed to describe the …
The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From the Eurofever Registry
NM ter Haar, J Jeyaratnam, HJ Lachmann… - Arthritis and …, 2016 - zora.uzh.ch
OBJECTIVE: Mevalonate kinase deficiency (MKD) is a rare metabolic disease characterized
by recurrent inflammatory episodes. This study was undertaken to describe the genotype …
by recurrent inflammatory episodes. This study was undertaken to describe the genotype …
The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From the Eurofever Registry
NM ter Haar, J Jeyaratnam, HJ Lachmann… - Arthritis & …, 2016 - infona.pl
Objective Mevalonate kinase deficiency (MKD) is a rare metabolic disease characterized by
recurrent inflammatory episodes. This study was undertaken to describe the genotype …
recurrent inflammatory episodes. This study was undertaken to describe the genotype …
The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From the Eurofever Registry
NM ter Haar, J Jeyaratnam, HJ Lachmann… - ARTHRITIS & …, 2016 - iris.unibs.it
OBJECTIVE: Mevalonate kinase deficiency (MKD) is a rare metabolic disease characterized
by recurrent inflammatory episodes. This study was undertaken to describe the genotype …
by recurrent inflammatory episodes. This study was undertaken to describe the genotype …
The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From the Eurofever Registry
NM ter Haar, J Jeyaratnam, HJ Lachmann… - ARTHRITIS & …, 2016 - arpi.unipi.it
Objective: Mevalonate kinase deficiency (MKD) is a rare metabolic disease characterized by
recurrent inflammatory episodes. This study was undertaken to describe the genotype …
recurrent inflammatory episodes. This study was undertaken to describe the genotype …
The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From the Eurofever Registry
NM ter Haar, J Jeyaratnam, HJ Lachmann… - Arthritis & …, 2016 - Wiley Online Library
Objective Mevalonate kinase deficiency (MKD) is a rare metabolic disease characterized by
recurrent inflammatory episodes. This study was undertaken to describe the genotype …
recurrent inflammatory episodes. This study was undertaken to describe the genotype …
[引用][C] The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From the Eurofever Registry
NM ter Haar, J Jeyaratnam, HJ Lachmann… - Arthritis & …, 2016 - cir.nii.ac.jp
The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From
the Eurofever Registry | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] …
the Eurofever Registry | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] …