Works matching Glucose-galactose malabsorption

Results: 63

Nephrocalcinosis in glucose-galactose malabsorption, association with renal tubular acidosis.

Published in:

Pediatric Nephrology, 2005, v. 20, n. 9, p. 1336, doi. 10.1007/s00467-005-1885-x

By:

El-Naggar, Walid;
Balfe, J. Williamson;
Barbar, Maha;
Taha, Doris

Publication type:

Article

SLC5A1 Variants in Turkish Patients with Congenital Glucose-Galactose Malabsorption.

Published in:

Genes, 2023, v. 14, n. 7, p. 1359, doi. 10.3390/genes14071359

By:

Hoşnut, Ferda Ö.;
Janecke, Andreas R.;
Şahin, Gülseren;
Vogel, Georg F.;
Lafcı, Naz G.;
Bichler, Paul;
Müller, Thomas;
Huber, Lukas A.;
Valovka, Taras;
Aksu, Aysel Ü.

Publication type:

Article

Congenital glucose‐galactose malabsorption: A case report with a novel SLC5A1 mutation.

Published in:

Clinical Case Reports, 2019, v. 7, n. 1, p. 51, doi. 10.1002/ccr3.1913

By:

Al‐lawama, Manar;
Albaramki, Jumana;
Altamimi, Mutaz;
El‐Shanti, Hatem

Publication type:

Article

Nephrocalcinosis in glucose-galactose malabsorption: nephrocalcinosis and proximal tubular dysfunction in a young infant with a novel mutation of SGLT1.

Published in:

2008

By:

Soylu, Özlem Bekem;
Ecevit, Çiğdem;
Altınöz, Serdar;
Öztürk, Aysel Aydoğan;
Temizkan, Ali Kemal;
Maeda, Mari;
Kasahara, Michihiro;
Soylu, Ozlem Bekem;
Ecevit, Ciğdem;
Altinöz, Serdar;
Oztürk, Aysel Aydoğan

Publication type:

journal article

Fructose Metabolism and Its Effect on Glucose-Galactose Malabsorption Patients: A Literature Review.

Published in:

Diagnostics (2075-4418), 2023, v. 13, n. 2, p. 294, doi. 10.3390/diagnostics13020294

By:

Alruwaili, Nawaf W.;
Alshdayed, Fahad

Publication type:

Article

Konjenital Glukoz-Galaktoz Malabsorbsiyonu ve Tekrarlayan Sepsis Atakları Olan Yenidoğan Olgusu.

Published in:

Journal of Current Pediatrics / Guncel Pediatri, 2013, v. 11, n. 2, p. 85, doi. 10.4274/Jcp.11.21931

By:

Alan, Serdar;
Kuloğlu, Zarife;
Çakır, Ufuk;
Yaman, Aytaç;
Atasay, Begüm;
Tanca, Aydan Kansu;
Arsan, Saadet

Publication type:

Article

Nephrolithiasis in a child with glucose-galactose malabsorption.

Published in:

Pediatric Nephrology, 2004, v. 19, n. 2, p. 244, doi. 10.1007/s00467-003-1327-6

By:

Tasic, Velibor;
Blau, Nenad;
Slaveska, Nevenka;
Santer, René

Publication type:

Article

Two Cases of Mistaken Polyuria and Nephrocalcinosis in Infants with Glucose-Galactose Malabsorption: A Possible Role of 1,25(OH)2D3.

Published in:

Hormone Research in Paediatrics, 2017, v. 87, n. 4, p. 277, doi. 10.1159/000454951

By:

Fiscaletti, Melissa;
Lebel, Marie-Jeanne;
Alos, Nathalie;
Benoit, Geneviève;
Jantchou, Prévost

Publication type:

Article

Long-Term Dietary Changes in Subjects with Glucose Galactose Malabsorption Secondary to Biallelic Mutations of SLC5A1.

Published in:

Digestive Diseases & Sciences, 2021, v. 66, n. 12, p. 4414, doi. 10.1007/s10620-020-06792-4

By:

Chan, Alvin P.;
Namjoshi, Shweta S.;
Jardack, Patricia M.;
Maloney, Lisa;
Ardjmand, Atrin;
Jackson, Nicholas N.;
Martin, Martin G.

Publication type:

Article

Dziedziczne zaburzenie wchłaniania glukozy i galaktozy.

Published in:

Gastroenterologia Polska / Gastroenterology, 2008, v. 15, n. 4, p. 241

By:

Korczowski, Bartosz;
Socha, Jerzy

Publication type:

Article

Structural Insights into Genetic Variants of Na/Glucose Cotransporter SGLT1 Causing Glucose-Galactose Malabsorption: vSGLT as a Model Structure.

Published in:

Cell Biochemistry & Biophysics, 2012, v. 63, n. 2, p. 151, doi. 10.1007/s12013-012-9352-3

By:

Raja, Mobeen;
Kinne, Rolf

Publication type:

Article

GLUCOSE-GALACTOSE MALABSORPTION.

Published in:: Nutrition Reviews, 1974, v. 32, n. 5, p. 132, doi. 10.1111/j.1753-4887.1974.tb06301.x
Publication type:: Article

SLC5A1 Mutations in Saudi Arabian Patients With Congenital Glucose-Galactose Malabsorption.

Published in:

2018

By:

Al-Suyufi, Yasir;
ALSaleem, Khalid;
Al-Mehaidib, Ali;
Banemai, Mohammed;
Aldekhail, Wajeeh M.;
Al-Muhandes, Abdulhakim;
Mohammed, Manal;
Allam, Rabab;
Jambi, Amani;
Ramzan, Khushnooda;
Imtiaz, Faiqa

Publication type:

journal article

The Molecular Basis of Glucose Galactose Malabsorption in a Large Swedish Pedigree.

Published in:

Function, 2021, v. 2, n. 5, p. 1, doi. 10.1093/function/zqab040

By:

Lostao, M Pilar;
Loo, Donald D;
Hernell, Olle;
Meeuwisse, Gunnar;
Martin, Martin G;
Wright, Ernest M

Publication type:

Article

Congenital glucose-galactose malabsorption: a novel deletion within the SLC5A1 gene.

Published in:

European Journal of Pediatrics, 2013, v. 172, n. 3, p. 409, doi. 10.1007/s00431-012-1802-9

By:

Vallaeys, L.;
Biervliet, S.;
Bruyn, G.;
Loeys, B.;
Moring, A.;
Deynse, E.;
Cornette, L.

Publication type:

Article

Literature review on congenital glucose–galactose malabsorption from 2001 to 2019.

Published in:

Journal of Paediatrics & Child Health, 2020, v. 56, n. 11, p. 1779, doi. 10.1111/jpc.14702

By:

Wang, Weiyan;
Wang, Liang;
Ma, Ming

Publication type:

Article

Congenital Glucose-Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene.

Published in:

2017

By:

Atay, Funda;
Derme, Turan;
Uras, Nurdan;
Ceylaner, Gulay;
Ceylaner, Serdar;
Sari, Fatma;
Oguz, Serife;
Atay, Funda Yavanoglu;
Sari, Fatma Nur;
Oguz, Serife Suna

Publication type:

journal article

Multiple sequence variations in SLC5A1 gene are associated with glucose-galactose malabsorption in a large cohort of Old Order Amish.

Published in:

Clinical Genetics, 2011, v. 79, n. 1, p. 86, doi. 10.1111/j.1399-0004.2010.01440.x

By:

Xin, B.;
Wang, H.

Publication type:

Article

Neonatal nephrocalcinosis in association with glucose-galactose malabsorption.

Published in:

Pediatric Nephrology, 2003, v. 18, n. 7, p. 700, doi. 10.1007/s00467-003-1155-8

By:

Pahari, Amitava;
Milla, Peter J.;
van't Hoff, William G.

Publication type:

Article

Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter.

Published in:

Nature, 1991, v. 350, n. 6316, p. 354

By:

Turkheimer, E.;
Zabel, B.

Publication type:

Article

Glucose-Galactose Malabsorption: A Study on the Transfer of Glucose Across the Red Cell Membrane.

Published in:

Scandinavian Journal of Clinical & Laboratory Investigation, 1970, v. 25, n. 2, p. 145, doi. 10.3109/00365517009049196

By:

Meeuwisse, G. W.

Publication type:

Article

PRENATAL IDENTIFICATION OF A HETEROZYGOUS STATUS IN TWO FETUSES AT RISK FOR GLUCOSE-GALACTOSE MALABSORPTION.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 5, p. 458, doi. 10.1002/(SICI)1097-0223(199605)16:5<458::AID-PD873>3.0.CO;2-U

By:

MARTÍN, MARTÍN G.;
TURK, ERIC;
KERNER, CYNTHIA;
ZABEL, BERNARD;
WIRTH, STEFAN;
WRIGHT, ERNEST M.

Publication type:

Article

Five Arab children with glucose-galactose malabsorption.

Published in:

Paediatrics & International Child Health, 2013, v. 33, n. 2, p. 108, doi. 10.1179/2046905513Y.0000000055

By:

Assiri, Asaad;
Saeed, Anjum;
Alnimri, Abdulrehman;
Ahmad, Sarfaraz;
Saeed, Elshazalay;
Jameel, Sajjad

Publication type:

Article

Congenital glucose-galactose malabsorption diagnosed from macrohematuria in an infant.

Published in:

Pediatrics International, 2016, v. 58, n. 12, p. 1365, doi. 10.1111/ped.13047

By:

Yoshimura, Ryoko;
Fujii, Tohru;
Endo, Amane;
Kudo, Takahiro;
Shimizu, Toshiaki

Publication type:

Article

GLUCOSE-GALACTOSE MALABSORPTION.

Published in:

Acta Paediatrica, 1969, v. 58, n. S188, p. 3, doi. 10.1111/j.1651-2227.1969.tb06045.x

By:

MEEUWISSE, G. W.;
MELIN, K.

Publication type:

Article

GLUCOSE-GALACTOSE MALABSORPTION.

Published in:

Acta Paediatrica, 1969, v. 58, n. S188, p. 19, doi. 10.1111/j.1651-2227.1969.tb06046.x

By:

MELIN, K.;
MEEUWISSE, G. W.

Publication type:

Article

GLUCOSE-GALACTOSE MALABSORPTION A Study with Biopsy of the Small Intestinal Mucosa.

Published in:

Acta Paediatrica, 1968, v. 57, n. 4, p. 273, doi. 10.1111/j.1651-2227.1968.tb07291.x

By:

Meeuwisse, G. W.;
Dahlqvist, A.

Publication type:

Article

Congenital Glucose-Galactose Malabsorption in a Child.

Published in:

2022

By:

Prasad, B. S.;
Yachha, Surender Kumar

Publication type:

Letter

Diagnosis of congenital glucose-galactose malabsorption by measuring sugar- and amino acid-evoked potential differences in jejunum in vivo.

Published in:

1986

By:

Igarashi, Y.;
Ohkohchi, N.;
Kikuta, A.;
Suzuki, J.;
Tada, K.

Publication type:

journal article

Digestion and absorption rates of lactose, glucose, galactose, and fructose in three infants with congenital glucose-galactose malabsorption: perfusion studies.

Published in:

1985

By:

Beyreiss, K.;
Hoepffner, W.;
Scheerschmidt, G.;
Müller, F.

Publication type:

journal article

Congenital Glucose-Galactose Malabsorption in a Neonate with Hyperbilirubinemia and Hypernatremia.

Published in:

2023

By:

Zhang, Fanhui;
Wang, Dandan;
Pan, Jiarong;
Chen, Lihua;
Yuan, Tianming

Publication type:

Letter

DIAGNOSTIC PROBLEMS IN GLUCOSE-GALACTOSE MALABSORPTION: A Case Report.

Published in:

Acta Paediatrica, 1970, v. 59, n. 2, p. 214, doi. 10.1111/j.1651-2227.1970.tb08992.x

By:

KAIJSER, K.;
ÖCKERMAN, P. A.

Publication type:

Article

GLUCOSE-GALACTOSE MALABSORPTION.

Published in:

Acta Paediatrica, 1970, v. 59, n. 1, p. 74, doi. 10.1111/j.1651-2227.1970.tb15517.x

By:

MEEUWISSE, G. W.;
LINDQUIST, B.

Publication type:

Article

A Case of Glucose-Galactose Malabsorption.

Published in:

Pediatrics International, 1977, v. 19, n. 2, p. 37, doi. 10.1111/j.1442-200X.1977.tb00092.x

By:

Kurosaka, Fumitake;
Uehara, Shinichiro;
Umezawa, Yoshiro;
Matunaga, Yoshinori;
Yamamoto, Matakazu

Publication type:

Article

Ensiling and hydrothermal pretreatment of grass: consequences for enzymatic biomass conversion and total monosaccharide yields.

Published in:

Biotechnology for Biofuels, 2014, v. 7, n. 1, p. 2, doi. 10.1186/1754-6834-7-95

By:

Ambye-Jensen, Morten;
Johansen, Katja S.;
Didion, Thomas;
Kádár, Zsófia;
Meyer, Anne S.

Publication type:

Article

A novel mutation of Na+/glucose cotransporter in a Turkish newborn with congenital glucose-galactose malabsorption.

Published in:

2005

By:

Gok, Faysal;
Aydin, Halil I;
Kurt, Ismail;
Gokcay, Erdal;
Maeda, Mari;
Kasahara, Michihiro

Publication type:

journal article

A Novel Mutation of Na+/Glucose Cotransporter in a Turkish Newborn with Congenital Glucose-Galactose Malabsorption.

Published in:

Journal of Pediatric Gastroenterology & Nutrition, 2005, v. 40, n. 4, p. 508, doi. 10.1097/01.MPG.0000153097.73083.A3

By:

Faysal Gok

Publication type:

Article

Congenital glucose-galactose malabsorption in Arab children.

Published in:

1996

By:

Abdullah, Assad M. A.;
El-Mouzan, Mohamed I.;
Shiekh, Omer Karrar El;
Mazyad, Abdullah Al;
Abdullah, A M;
el-Mouzan, M I;
el Shiekh, O K;
al Mazyad, A

Publication type:

journal article

Congenital fructose-glucose-galactose malabsorption.

Published in:

1995

By:

Iacono, G.;
Carroccio, A.;
Cavataio, F.;
Montalto, G.;
Soresi, M.

Publication type:

journal article

19 GLUCOSE-GALACTOSE MALABSORPTION ASSOCIATED WITH MULTIPLE MUTATIONS IN THE Na+/GLUCOSE COTRANSPORTER.

Published in:

Journal of Pediatric Gastroenterology & Nutrition, 1994, v. 19, n. 3, p. 334

By:

Turk, E;
Kachulis, C;
Wright, E M

Publication type:

Article

Konjenital glukoz-galaktoz malabsorpsiyonu: Bir yenidoğan vakası.

Published in:

Cocuk Sagligi ve Hastaliklari Dergisi, 2015, v. 58, n. 1, p. 28

By:

Törer, Birgin;
Çetinkaya, Bilin;
Hanta, Deniz;
Canan, Oğuz;
Gülcan, Hande

Publication type:

Article

Glucose transporters in the small intestine in health and disease.

Published in:

Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 9, p. 1207, doi. 10.1007/s00424-020-02439-5

By:

Koepsell, Hermann

Publication type:

Article

Importance of Early Genetic Sequencing in Neonates Admitted to NICU with Recurrent Hypernatremia: Results of a Prospective Cohort Study.

Published in:

Neonatology (16617800), 2022, v. 119, n. 1, p. 103, doi. 10.1159/000519634

By:

Hu, Liyuan;
Yang, Lin;
Yan, Kai;
Wu, Bingbing;
Wang, Huijun;
Zhang, Rong;
Wang, Jin;
Cao, Yun;
Cheng, Guoqiang;
Zhou, Wenhao

Publication type:

Article

Active sugar transport in health and disease.

Published in:

Journal of Internal Medicine, 2007, v. 261, n. 1, p. 32, doi. 10.1111/j.1365-2796.2006.01746.x

By:

Wright, E. M.;
Hirayama, B. A.;
Loo, D. F.

Publication type:

Article

Diagnosing and Treating Intolerance to Carbohydrates in Children.

Published in:

Nutrients, 2016, v. 8, n. 3, p. 157, doi. 10.3390/nu8030157

By:

Pezzella, Vincenza;
Amoroso, Antonio;
Cozzolino, Tommaso;
Di Scala, Carmen;
Passariello, Annalisa;
Canani, Roberto Berni

Publication type:

Article

What does sodium‐glucose co‐transporter 1 inhibition add: Prospects for dual inhibition.

Published in:

Diabetes, Obesity & Metabolism, 2019, v. 21, p. 43, doi. 10.1111/dom.13630

By:

Dominguez Rieg, Jessica A.;
Rieg, Timo

Publication type:

Article

Prokaryotic Solute/Sodium Symporters: Versatile Functions and Mechanisms of a Transporter Family †.

Published in:

International Journal of Molecular Sciences, 2021, v. 22, n. 4, p. 1880, doi. 10.3390/ijms22041880

By:

Henriquez, Tania;
Wirtz, Larissa;
Su, Dan;
Jung, Heinrich;
Frillingos, Stathis;
Botou, Maria

Publication type:

Article

Enteroendocrine Dysfunction in Two Saudi Sisters.

Published in:

Case Reports in Gastroenterology, 2021, v. 15, n. 1, p. 290, doi. 10.1159/000511761

By:

Ahmed, Amna Basheer M.;
Alsaleem, Badr M. Rasheed

Publication type:

Article

Lactose malabsorption in young Lithuanian children with atopic dermatitis.

Published in:

Acta Paediatrica, 2004, v. 93, n. 4, p. 482

By:

Rudzeviciene, O.;
Narkeviciute, I.;
Eidukevicius, R.

Publication type:

Article

Antidepressant binding site in a bacterial homologue of neurotransmitter transporters.

Published in:

Nature, 2007, v. 448, n. 7156, p. 952, doi. 10.1038/nature06038

By:

Singh, Satinder K.;
Yamashita, Atsuko;
Gouaux, Eric

Publication type:

Article