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Results for
""Liddle Syndrome""[mesh_terms]

18 Results

Searching titles within these results

Molecular genetics of Liddle's syndrome.

Kun-Qi Yang, Xian-Liang Zhou, Yan Xiao, Tao Tian, Ling-Gen Gao

Clinica chimica acta; international journal of clinical chemistry 2015;436():202-6

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Liddle syndrome with a SCNN1B mutation: a case report and systematic review.

Qian Tang, Yangfan Zhou, Lin Liu, Min Chen, Lin Liu, Yan Wang, Guangju Zhou, Meijun Xie

BMC nephrology 2025;26(1):408

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Inherited forms of mineralocorticoid hypertension.

Maria-Christina Zennaro, Sheerazed Boulkroun, Fabio Fernandes-Rosa

Best practice & research. Clinical endocrinology & metabolism 2016;29(4):633-45

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Liddle Syndrome: Review of the Literature and Description of a New Case.

Martina Tetti, Silvia Monticone, Jacopo Burrello, Patrizia Matarazzo, Franco Veglio, Barbara Pasini, Xavier Jeunemaitre, Paolo Mulatero

International journal of molecular sciences 2018;19(3):812

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A frameshift mutation in the gene in a family with Liddle syndrome: A case report and systematic review.

Yiting Lu, Xinchang Liu, Lin Sun, Di Zhang, Peng Fan, Kunqi Yang, Lin Zhang, Yaxin Liu, Xianliang Zhou

Molecular medicine reports 2023;29(2):19

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Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension.

Peng Fan, Xiao-Cheng Pan, Di Zhang, Kun-Qi Yang, Ying Zhang, Tao Tian, Fang Luo, Wen-Jun Ma, Ya-Xin Liu, Lin-Ping Wang, Hui-Min Zhang, Lei Song, Jun Cai, Xian-Liang Zhou

American journal of hypertension 2021;33(7):670-675

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Liddle Syndrome with a SCNN1A Mutation: A Case Report and Literature Review.

Xueyi Wu, Fei Xiang, Li Ma, Jiajia Tian, Liandi Wang, Lijuan Shao, Chuwen Fang

Kidney & blood pressure research 2024;49(1):831-838

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Low-Renin Hypertension.

Shobana Athimulam, Natalia Lazik, Irina Bancos

Endocrinology and metabolism clinics of North America 2020;48(4):701-715

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A parent and child with Liddle syndrome diagnosed correctly with the child as the proband: a case report with review of literature.

Shinichi Uchida, Eisei Sohara, Satoshi Morita, Minako Tokunaga, Yuko Seki, Tatsushi Horiguchi, Kiwako Miura, Haruna Kakimoto, Michiyo Mizota, Koshi Kusumoto, Takayasu Mori, Yasuhiro Okamoto

Endocrine journal 2025;72(3):319-323

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Monogenic Forms of Hypertension.

Filippo Ceccato, Franco Mantero

Endocrinology and metabolism clinics of North America 2020;48(4):795-810

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Inherited forms of mineralocorticoid hypertension.

Paul M Stewart, Zaki Hassan-Smith

Current opinion in endocrinology, diabetes, and obesity 2012;18(3):177-85

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Liddle syndrome in a Serbian family and literature review of underlying mutations.

Radovan Bogdanović, Vladimir Kuburović, Nataša Stajić, Sadaf S Mughal, Alina Hilger, Sanja Ninić, Sergej Prijić, Michael Ludwig

European journal of pediatrics 2012;171(3):471-8

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Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome.

Kun-Qi Yang, Chao-Xia Lu, Peng Fan, Ying Zhang, Xu Meng, Xue-Qi Dong, Fang Luo, Ya-Xin Liu, Hui-Min Zhang, Hai-Ying Wu, Jun Cai, Xue Zhang, Xian-Liang Zhou

Clinical and experimental hypertension (New York, N.Y. : 1993) 2018;40(2):107-111

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Genetic disorders of potassium homeostasis.

Gaurav Jain, Song Ong, David G Warnock

Seminars in nephrology 2014;33(3):300-9

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Identification of glycyrrhizin metabolites in humans and of a potential biomarker of liquorice-induced pseudoaldosteronism: a multi-centre cross-sectional study.

Kanon Takahashi, Tetsuhiro Yoshino, Yasuhito Maki, Kan'ichiro Ishiuchi, Takao Namiki, Keiko Ogawa-Ochiai, Kiyoshi Minamizawa, Toshiaki Makino, Tomonori Nakamura, Masaru Mimura, Kenji Watanabe

Archives of toxicology 2020;93(11):3111-3119

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Results: 1 – 15 / 18

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Results for ""Liddle Syndrome""[mesh_terms]

Molecular genetics of Liddle's syndrome.

Liddle syndrome with a SCNN1B mutation: a case report and systematic review.

Inherited forms of mineralocorticoid hypertension.

Liddle Syndrome: Review of the Literature and Description of a New Case.

A frameshift mutation in the gene in a family with Liddle syndrome: A case report and systematic review.

Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension.

Liddle Syndrome with a SCNN1A Mutation: A Case Report and Literature Review.

Low-Renin Hypertension.

A parent and child with Liddle syndrome diagnosed correctly with the child as the proband: a case report with review of literature.

Monogenic Forms of Hypertension.

Inherited forms of mineralocorticoid hypertension.

Liddle syndrome in a Serbian family and literature review of underlying mutations.

Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome.

Genetic disorders of potassium homeostasis.

Identification of glycyrrhizin metabolites in humans and of a potential biomarker of liquorice-induced pseudoaldosteronism: a multi-centre cross-sectional study.

Results for
""Liddle Syndrome""[mesh_terms]