GAMT deficiency: features, treatment, and outcome in an inborn error of creatine synthesis

S Mercimek-Mahmutoglu, S Stoeckler-Ipsiroglu… - Neurology, 2006 - AAN Enterprises
Background: Guanidinoactetate methyltransferase (GAMT) deficiency is an autosomal
recessive disorder of creatine synthesis. The authors analyzed clinical, biochemical, and …
被引用次数：193 相关文章

[引用][C] GAMT deficiency: Features, treatment, and outcome in an inborn error of creatine synthesis

S MERCIMEK-MAHMUTOGLU… - …, 2006 - pascal-francis.inist.fr
Author MERCIMEK-MAHMUTOGLU, S 1; STOECKLER-IPSIROGLU, S 1; ITEM, C. B 10;
LEUZZI, V 11; MARQUARDT, I 12; MÜHL, A 10; SAELKE-KELLERMANN, R. A 13; …

GAMT deficiency: Features, treatment, and outcome in an inborn error of creatine synthesis

S Mercimek-Mahmutoglu… - …, 2006 - researchinformation.amsterdamumc …
BACKGROUND: autosomal recessive disorder of creatine synthesis. The authors analyzed
clinical, biochemical, and molecular findings in 27 patients. METHODS: The authors …

GAMT deficiency: features, treatment, and outcome in an inborn error of creatine synthesis.

S Mercimek-Mahmutoglu, S Stoeckler-Ipsiroglu… - Neurology, 2006 - europepmc.org
Background Guanidinoactetate methyltransferase (GAMT) deficiency is an autosomal
recessive disorder of creatine synthesis. The authors analyzed clinical, biochemical, and …

Features, treatment, and outcome in an inborn error of creatine synthesis

S Mercimek-Mahmutoglu, S Stoeckler-Ipsiroglu… - 2006 - publications.goettingen-research …
Background: Guanidinoactetate methyltransferase (GAMT) deficiency is an autosomal
recessive disorder of creatine synthesis. The authors analyzed clinical, biochemical, and …

GAMT deficiency: features, treatment, and outcome in an inborn error of creatine synthesis

S Mercimek-Mahmutoglu… - …, 2006 - pubmed.ncbi.nlm.nih.gov
Background Guanidinoactetate methyltransferase (GAMT) deficiency is an autosomal
recessive disorder of creatine synthesis. The authors analyzed clinical, biochemical, and …

GAMT deficiency

S Mercimek-Mahmutoglu, S Stoeckler-Ipsiroglu… - Neurology, 2006 - cir.nii.ac.jp
GAMT deficiency | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ
移動 検索フォームへ移動 論文・データをさがす 大学図書館の本をさがす 日本の博士論文をさがす …

GAMT deficiency: Features, treatment, and outcome in an inborn error of creatine synthesis

S Mercimek Mahmutoglu, S Stoeckler Ipsiroglu… - …, 2006 - iris.uniroma1.it
BACKGROUND: autosomal recessive disorder of creatine synthesis. The authors analyzed
clinical, biochemical, and molecular findings in 27 patients. METHODS: The authors …

[引用][C] GAMT deficiency features, treatment, and outcome in an inborn error of creatine synthesis

S MERCOMEK-MAHMUTOGLU - Neurology, 2006 - cir.nii.ac.jp

[引用][C] GAMT deficiency: Features, treatment, and outcome in an inborn error of creatine synthesis

S MERCIMEK-MAHMUTOGLU… - …, 2006 - Lippincott Williams & Wilkins