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Items: 1 to 20 of 117

1.
Concurrence of Hyperhidrosis and Hypohidrosis in Ross Syndrome
Gracia Hamadeh, Jawad Fares
Clin Med Res. 2023 Mar; 21(1): 49–52. doi: 10.3121/cmr.2022.1780
PMCID:
PMC10153678
ArticlePDF–1.0M
2.
Pharmacovigilance-based drug repurposing: searching for putative drugs with hypohidrosis or anhidrosis adverse events for use against hyperhidrosis
Yi Liu, Yanguo Liu, Rongrong Fan, Nurmuhammat Kehriman, Xiaohong Zhang, Bin Zhao, Lin Huang
Eur J Med Res. 2023; 28: 95. Published online 2023 Feb 24. doi: 10.1186/s40001-023-01048-z
PMCID:
PMC9951540
ArticlePDF–2.5M
3.
A Mutation in the Tubulin-Encoding TUBB3 Gene Causes Complex Cortical Malformations and Unilateral Hypohidrosis
Shinobu Fukumura, Mitsuhiro Kato, Kentaro Kawamura, Akiko Tsuzuki, Hiroyuki Tsutsumi
Child Neurol Open. 2016 Jan-Dec; 3: 2329048X16665758. Published online 2016 Sep 1. doi: 10.1177/2329048X16665758
PMCID:
PMC5417280
ArticlePDF–311K
4.
First case of congenital idiopathic hypohidrosis in China
Ge Shi, Cheng-Yao Zhu, Ying Zhou, Yan-Ping Yang, Yi-Ming Fan
An Bras Dermatol. 2015 Sep-Oct; 90(5): 731–733. doi: 10.1590/abd1806-4841.20153327
PMCID:
PMC4631239
ArticlePDF–263K
5.
Evaluation of Sweat Production by Pilocarpine Iontophoresis: A Noninvasive Screening Tool for Hypohidrosis in Ectodermal Dysplasia
Surupa Basu, Monjori Mitra, Apurba Ghosh
Indian J Clin Biochem. 2013 Oct; 28(4): 433–435. Published online 2013 May 15. doi: 10.1007/s12291-013-0334-z
PMCID:
PMC3783914
ArticlePDF–182K
6.
Granulysin-Bearing Cells in the Skin Lesions of Acute Graft-versus-Host Disease: Possible Mechanisms for Hypohidrosis in Graft-versus-Host Disease
Sadanori Furudate, Taku Fujimura, Yumi Kambayashi, Setsuya Aiba
Case Rep Dermatol. 2013 Jan-Apr; 5(1): 93–98. Published online 2013 Apr 5. doi: 10.1159/000350561
PMCID:
PMC3635966
ArticlePDF–811K
7.
Efficacy of Stellate Ganglion Block in Cholinergic Urticaria with Acquired Generalized Hypohidrosis
Jee Hyun Shin, Do Wan Kim, Jong Yeun Yang, Won Il Lee
Korean J Pain. 2012 Oct; 25(4): 278–280. Published online 2012 Oct 4. doi: 10.3344/kjp.2012.25.4.278
PMCID:
PMC3468808
ArticlePDF–230K
8.
MicroRNA-155 expression with Brucella infection in vitro and in vivo and decreased serum levels of MicroRNA-155 in patients with brucellosis
Xi Zhang, Jingjing Chen, Huimin Cheng, Jinying Zhu, Qiao Dong, Huan Zhang, Zeliang Chen
Sci Rep. 2022; 12: 4181. Published online 2022 Mar 9. doi: 10.1038/s41598-022-08180-6
PMCID:
PMC8907217
ArticlePDF–1.3M
9.
Intra-auricular modification of facelift incision decreased the risk of Frey syndrome
Chih-Ying Chen, Peir-Rong Chen, Yu-Fu Chou
Tzu Chi Med J. 2019 Oct-Dec; 31(4): 266–269. Published online 2019 Sep 16. doi: 10.4103/tcmj.tcmj_117_18
PMCID:
PMC6905232
ArticlePDF–705K
10.
Gross Cystic Disease Fluid Protein 15 in Stratum Corneum Is a Potential Marker of Decreased Eccrine Sweating for Atopic Dermatitis
Koji Kamiya, Jun-Ichi Sakabe, Hayato Yamaguchi, Takahiro Suzuki, Tsuyoshi Yatagai, Masahiro Aoshima, Taisuke Ito, Yoshiki Tokura
PLoS One. 2015; 10(4): e0125082. Published online 2015 Apr 28. doi: 10.1371/journal.pone.0125082
PMCID:
PMC4412570
ArticlePDF–1.1M
11.
Chronic eosinophilic pneumonia with persistent decreased diffusing capacity for carbon monoxide
Sibylle Blanc, Marc Albertini, Sylvie Leroy, Lisa Giovannini-Chami
BMJ Case Rep. 2013; 2013: bcr2012008238. Published online 2013 Feb 15. doi: 10.1136/bcr-2012-008238
PMCID:
PMC3604399
ArticlePDF–236K
12.
Cystic fibrosis patients bearing both the common missense mutation, Gly→Asp at codon 551 and the ΔF508 mutation are clinically indistinguishable from ΔF508 homozygotes, except for decreased risk of meconium ileus
Ada Hamosh, Terri M. King, Beryl J. Rosenstein, Mary Corey, Henry Levison, Peter Durie, Lap-Chee Tsui, Iain McIntosh, Marion Keston, David J. H. Brock, Milan Macek, Dana Zemková, Hana Krásničanová, Věra Vávrová, Milan Macek, Neil Golder, Martin J. Schwarz, Maurice Super, Eila K. Watson, Carolyn Williams, Andrew Bush, Sinead M. O'Mahoney, Peter Humphries, Miguel A. DeArce, André Reis, Joachim Bürger, Manfred Stuhrmann, Jörg Schmidtke, Ulrich Wulbrand, Thilo Dörk, Burkhard Tümmler, Garry R. Cutting
Am J Hum Genet. 1992 Aug; 51(2): 245–250.
PMCID:
PMC1682672
SummaryPage BrowsePDF–800K
13.
A neuropathic deficit, decreased sweating, is prevented and ameliorated by euglycemia in streptozocin diabetes in rats.
C Cardone, P J Dyck
J Clin Invest. 1990 Jul; 86(1): 248–253. doi: 10.1172/JCI114691
PMCID:
PMC296714
SummaryPage BrowsePDF–1.2M
14.
Basan gets a new fingerprint: Mutations in the skin-specific isoform of SMARCAD1 cause ectodermal dysplasia syndromes with adermatoglyphia
Monica N. Valentin, Benjamin D. Solomon, Gabriele Richard, Carlos R. Ferreira, A. Yasmine Kirkorian
Am J Med Genet A. Author manuscript; available in PMC 2023 Oct 6.
Published in final edited form as: Am J Med Genet A. 2018 Nov; 176(11): 2451–2455. Published online 2018 Oct 5. doi: 10.1002/ajmg.a.40485
PMCID:
PMC10557913
ArticlePDF–2.1M
15.
Molecular Modeling Analysis Provides Genotype–Phenotype Correlation Insights in a Patient with Ankyloblepharon-Ectodermal Dysplasia-Clefting Syndrome
Anna Douka, Lambros Goutzanis, Dimitrios Vlachakis, George P. Chrousos, Christos Yapijakis
Genes (Basel) 2023 Jun; 14(6): 1246. Published online 2023 Jun 10. doi: 10.3390/genes14061246
PMCID:
PMC10298433
ArticlePDF–2.9M
16.
Mutations within the putative protease domain of the human FAM111B gene may predict disease severity and poor prognosis: A review of POIKTMP cases
Afolake Arowolo, Cenza Rhoda, Nonhlanhla Khumalo
Exp Dermatol. 2022 May; 31(5): 648–654. Published online 2022 Feb 13. doi: 10.1111/exd.14537
PMCID:
PMC9344908
ArticlePDF–1.1M
17.
Clinical and genetic spectrum in Chinese families with Fabry disease: a single‐centre case series
Xin Chen, Hezhi Li, Hongtao Liao, Xianzhang Zhan, Zhian Zhong, Qianhuan Zhang, Lie Liu, Yuanhong Liang, Hai Deng, Xianhong Fang, Yumei Xue, Shulin Wu, Yang Liu
ESC Heart Fail. 2021 Dec; 8(6): 5436–5444. Published online 2021 Oct 26. doi: 10.1002/ehf2.13638
PMCID:
PMC8712914
ArticlePDF–16M
18.
Multidisciplinary approach to screening and management of children with Fabry disease: practice at a Tertiary Children’s Hospital in China
Qian Shen, Jialu Liu, Jing Chen, Shuizheng Zhou, Yi Wang, Lifei Yu, Li Sun, Liuhui Wang, Bingbing Wu, Fang Liu, Yun Cao, Ying Huang, Jianshe Wang, Chenhao Yang, Daqian Zhu, Yangyang Ma, Zhengmin Xu, Wei Lu, Lili Fu, Wenhao Zhou, Hong Xu
Orphanet J Rare Dis. 2021; 16: 509. Published online 2021 Dec 14. doi: 10.1186/s13023-021-02136-1
PMCID:
PMC8670193
ArticlePDF–1.6M
19.
Novel missense mutation of the TP63 gene in a newborn with Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome: clinical report and follow-up
Gregorio Serra, Vincenzo Antona, Mario Giuffré, Federica Li Pomi, Lucia Lo Scalzo, Ettore Piro, Ingrid Anne Mandy Schierz, Giovanni Corsello
Ital J Pediatr. 2021; 47: 196. Published online 2021 Sep 28. doi: 10.1186/s13052-021-01152-y
PMCID:
PMC8479907
ArticlePDF–717K
20.
Gene Mutations of the Three Ectodysplasin Pathway Key Players (EDA, EDAR, and EDARADD) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations
Hoda A. Ahmed, Ghada Y. El-Kamah, Eman Rabie, Mostafa I. Mostafa, Maha R. Abouzaid, Nehal F. Hassib, Mennat I. Mehrez, Mohamed A. Abdel-Kader, Yasmine H. Mohsen, Suher K. Zada, Khalda S. Amr, Inas S. M. Sayed
Genes (Basel) 2021 Sep; 12(9): 1389. Published online 2021 Sep 8. doi: 10.3390/genes12091389
PMCID:
PMC8468066
ArticlePDF–6.2M

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