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Select item 83880431.

Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary Hypocalcemia

Elvan Bayramoğlu, Melikşah Keskin, Zehra Aycan, Şenay Savaş-Erdeve, Semra Çetinkaya

J Clin Res Pediatr Endocrinol. 2021 Sep; 13(3): 300–307. Published online 2021 Aug 23. doi: 10.4274/jcrpe.galenos.2021.2020.0192

PMCID:: PMC8388043

Abstract Article PDF–457K

Select item 3657162.

Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia

Vladimir Chubanov, Siegfried Waldegger, Michael Mederos y Schnitzler, Helga Vitzthum, Martin C. Sassen, Hannsjörg W. Seyberth, Martin Konrad, Thomas Gudermann

Proc Natl Acad Sci U S A. 2004 Mar 2; 101(9): 2894–2899. Published online 2004 Feb 19. doi: 10.1073/pnas.0305252101

PMCID:: PMC365716

Abstract Article PDF–545K

Select item 41817123.

Aceptabilidad del diagnóstico rápido casero para HIV entre hombres gay y otros hombres que tienen sexo con hombres (G&HSH) de la Ciudad de Buenos Aires

Iván C. Balán, Alex Carballo-Diéguez, Rubén O. Marone, María A. Pando, Victoria Barreda, María M. Ávila

Actual SIDA. Author manuscript; available in PMC 2014 Oct 1.

Published in final edited form as: Actual SIDA. 2011 Mar; 19(71): 26–32.

PMCID:: PMC4181712

Abstract Article PDF–48K

Select item 72191304.

A novel TRPM6 variant (c.3179T>A) causing familial hypomagnesemia with secondary hypocalcemia

Sara Lomelino-Pinheiro, Bastos Margarida, Adriana de Sousa Lages

Endocrinol Diabetes Metab Case Rep. 2020; 2020: 20-0005. Published online 2020 May 5. doi: 10.1530/EDM-20-0005

PMCID:: PMC7219130

Abstract Article PDF–897K

Select item 109854205.

A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant

Mohammed Shahab Uddin, AlZahra Y. Alradhi, Fahad Mushbb N. Alqathani, Othman Saleh Alessa, Ahmed Nawfal M. Alshammari, Ratna Tripathy, Mohammed Ahmed Alomari

Am J Case Rep. 2024; 25: e942498-1–e942498-10. Published online 2024 Mar 26. doi: 10.12659/AJCR.942498

PMCID:: PMC10985420

Abstract Article PDF–687K

Select item 63610886.

Exome sequencing identifies a novel frameshift variant causing hypomagnesemia with secondary hypocalcemia

M. Kamran Azim, Aisha Mehnaz, Javeria Z. Ahmed, Ghulam Mujtaba

CEN Case Rep. 2019 Feb; 8(1): 42–47. Published online 2018 Aug 24. doi: 10.1007/s13730-018-0362-x

PMCID:: PMC6361088

Abstract Article PDF–1.2M

Select item 64032177.

A pediatric case of hypomagnesemia 1 (HOMG1) caused by novel compound heterozygous mutations in TRPM6

Takeshi Goda, Hiroshi Komatsu, Kandai Nozu, Hisakazu Nakajima

Hum Genome Var. 2019; 6: 13. Published online 2019 Mar 6. doi: 10.1038/s41439-019-0043-0

PMCID:: PMC6403217

Abstract Article PDF–474K

Select item 31614108.

PREVENCIÓN DEL VIH/SIDA EN LOS CIRCUITOS DE LEVANTE HSH: UNA ASIGNATURA PENDIENTE

Victoria Barreda, Alex Carballo-Dieguez, Rubén Marone, Iván Balán, María Ángeles Pando, María Mercedes Ávila

Sex Salud Soc (Rio J) Author manuscript; available in PMC 2011 Aug 25.

Published in final edited form as: Sex Salud Soc (Rio J). 2010 Dec; (6): 41–62. doi: 10.1590/s1984-64872010000100003

PMCID:: PMC3161410

Abstract Article PDF–60K

Select item 39539059.

New TRPM6 missense mutations linked to hypomagnesemia with secondary hypocalcemia

Sergio Lainez, Karl Peter Schlingmann, Jenny van der Wijst, Bernd Dworniczak, Femke van Zeeland, Martin Konrad, René J Bindels, Joost G Hoenderop

Eur J Hum Genet. 2014 Apr; 22(4): 497–504. Published online 2013 Aug 14. doi: 10.1038/ejhg.2013.178

PMCID:: PMC3953905

Abstract Article PDF–1.2M

Select item 870261110.

Familial Hypomagnesemia With Secondary Hypocalcemia: A Case Report

Nour Gazzaz, Maha Alghamdi

Cureus. 2021 Nov; 13(11): e19847. Published online 2021 Nov 23. doi: 10.7759/cureus.19847

PMCID:: PMC8702611

Abstract Article PDF–86K

Select item 931524411.

Case Report: Novel TRPM6 Mutations Cause Hereditary Hypomagnesemia With Secondary Hypocalcemia in a Chinese Family and a Literature Review

Yiran Han, Yajuan Zhao, Hua Wang, Liang Huo

Front Pediatr. 2022; 10: 912524. Published online 2022 Jul 12. doi: 10.3389/fped.2022.912524

PMCID:: PMC9315244

Abstract Article PDF–2.9M

Select item 1045016412.

Structural basis for specific DNA sequence motif recognition by the TFAP2 transcription factors

Ke Liu, Yuqing Xiao, Linyao Gan, Weifang Li, Jin Zhang, Jinrong Min

Nucleic Acids Res. 2023 Aug 25; 51(15): 8270–8282. Published online 2023 Jul 6. doi: 10.1093/nar/gkad583

PMCID:: PMC10450164

Abstract Article PDF–1.6M

Select item 323834913.

Phosphatidylinositol 4,5-bisphosphate (PIP₂) controls magnesium gatekeeper TRPM6 activity

Jia Xie, Baonan Sun, Jianyang Du, Wenzhong Yang, Hsiang-Chin Chen, Jeffrey D. Overton, Loren W. Runnels, Lixia Yue

Sci Rep. 2011; 1: 146. Published online 2011 Nov 9. doi: 10.1038/srep00146

Correction in:: Sci Rep. 2012; 2: 559.

PMCID:: PMC3238349

Abstract Article PDF–2.0M

Select item 781150514.

Inherited forms of renal hypomagnesemia: an update

Nine V. A. M. Knoers

Pediatr Nephrol. 2009; 24(4): 697–705. Published online 2009 Apr 1. doi: 10.1007/s00467-008-0968-x

PMCID:: PMC7811505

Abstract Article PDF–247K

Select item 1033478415.

Cell surface nucleocapsid protein expression: A betacoronavirus immunomodulatory strategy

Alberto Domingo López-Muñoz, Jefferson J. S. Santos, Jonathan W. Yewdell

Proc Natl Acad Sci U S A. 2023 Jul 11; 120(28): e2304087120. Published online 2023 Jul 3. doi: 10.1073/pnas.2304087120

PMCID:: PMC10334784

Abstract Article PDF–1.7M

Select item 480504016.

A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case Report

Ayça Altıncık, Karl Peter Schlingmann, Mahya Sultan Tosun

J Clin Res Pediatr Endocrinol. 2016 Mar; 8(1): 101–104. Published online 2016 Mar 1. doi: 10.4274/jcrpe.2254

PMCID:: PMC4805040

Abstract Article PDF–126K

Select item 794772817.

Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation

Hüsniye Yücel, Çiğdem Genç Sel, Çiğdem Seher Kasapkara, Gülin Karacan Küçükali, Senay Savas-Erdeve, Ülkühan Öztoprak, Serdar Ceylaner, Saliha Şenel, Meltem Akçaboy

J Clin Res Pediatr Endocrinol. 2021 Mar; 13(1): 114–118. Published online 2021 Feb 26. doi: 10.4274/jcrpe.galenos.2020.2020.0004