Works matching DE "FAILURE to thrive syndrome"

Results: 703

ERAS ushers in new age of surgical care: 'Enhanced Recovery' protocols help maintain homeostasis, with multiple benefits.

Published in:

Urology Times, 2018, v. 46, n. 3, p. 1

By:

Hilton, Lisette

Publication type:

Article

Sweetness preferences in 1-year-old children who fail to thrive.

Published in:

Journal of Reproductive & Infant Psychology, 2001, v. 19, n. 3, p. 253, doi. 10.1080/02646830120073242

By:

Kasese-Hara, Mambwe;
Drewett, Robert;
Wright, Charlotte

Publication type:

Article

A Unique Case of Craniopagus Twins: Considerations and Challenges for Dental Rehabilitation.

Published in:

2013

By:

Campbell, Karen M.

Publication type:

Case Study

Infants and children who fail to thrive: Implications for occupational therapy practice.

Published in:

Occupational Therapy in Health Care, 1995, v. 9, n. 2/3, p. 91, doi. 10.1080/J003v09n02_06

By:

Wavrek, Barbara B.

Publication type:

Article

The nature and diversity of problems leading to failure to thrive.

Published in:

Occupational Therapy in Health Care, 1995, v. 9, n. 2/3, p. 73, doi. 10.1300/J003v09n02_05

By:

Humphry, Ruth

Publication type:

Article

Subclinical maculopathy and retinopathy in transcobalamin deficiency: a 10-year follow-up.

Published in:

Documenta Ophthalmologica, 2022, v. 144, n. 1, p. 53, doi. 10.1007/s10633-021-09849-5

By:

Rigaudière, Florence;
Nasser, Hala;
Delouvrier, Eliane;
Milani, Paolo;
Schiff, Manuel

Publication type:

Article

Giant Cardiac Fibroma: An Unusual Cause of Failure to Thrive.

Published in:

2013

By:

Navarini, Susanne;
Latzin, Philipp;
Kadner, Alexander;
Carrel, Thierry;
Hutter, Damian

Publication type:

Report

Diencephalic syndrome in a female child due to intracranial germinoma: a case report.

Published in:

2022

By:

Ju, Yan;
Liu, Peng;
Li, Li;
Zhou, Liangxue;
Liu, Xiaoyin;
He, Jiaojiang

Publication type:

Case Study

Hypercalcemia Secondary to Elevated PTHrP in an Infant Followed by Progression to Nephrotic Syndrome.

Published in:

JCEM Case Reports, 2024, v. 2, n. 5, p. 1, doi. 10.1210/jcemcr/luae074

By:

Gimeno, Alex F;
Hunley, Tracy E;
Kelley, Jennifer C

Publication type:

Article

A Case of Congenital Disorder of Glycosylation Type 1b Presenting as Hyperinsulinemic Hypoglycemia and Failure to Thrive.

Published in:

JCEM Case Reports, 2023, v. 1, n. 5, p. 1, doi. 10.1210/jcemcr/luad109

By:

Rani, Swati;
Sahai, Inderneel;
Misra, Madhusmita

Publication type:

Article

Persistent Hypoglycemia and Hyperinsulinism in a Patient With KMT2D-Associated Kabuki Syndrome.

Published in:

JCEM Case Reports, 2023, v. 1, n. 2, p. 1, doi. 10.1210/jcemcr/luad032

By:

Stosic, Mariana Nunez;
Gomez, Patricia

Publication type:

Article

Fructose Metabolism Defects in Indian Children - Uncommon or Under-reported? - a Case Series.

Published in:

Central European Journal of Paediatrics, 2023, v. 19, n. 2, p. 137, doi. 10.5457/p2005-114.348

By:

Mirza, Nida;
Maheshwari, Ankita

Publication type:

Article

'H-type' tracheoesophageal fistula in an infant: A case report.

Published in:

African Journal of Thoracic & Critcal Care Medicine, 2022, v. 28, n. 4, p. 195, doi. 10.7196/AJTCCM.2022.v28i4.203

By:

Moremi-Letsoalo, M. D.;
van As, A. B. (Sebastian);
Nchabeleng, R. M.;
Risenga, S.

Publication type:

Article

Congenital Anomalies of the Kidney and Urinary Tract a single center study.

Published in:

Kerbala Jorunal of Medicine, 2020, v. 13, n. 2, p. 2367

By:

Hassan, Faliha Obaid;
Edan, Ali Ibrahim;
Ubaidy, Mohamed Saad Al

Publication type:

Article

كاربرد تئورى شناختى اجتماعى بر رفتار تغذيه اى مادران و وزن كودكان 6 تا 12 ماهه مبتلا به اختلال رشد.

Published in:

Iranian Journal of Health Education & Health Promotion, 2021, v. 9, n. 2, p. 145, doi. 10.52547/ijhehp.9.2.145

By:

زينب اقدسى;
هادى طهرانى;
حبيب اله اسماعيل;
محدثه قوامى;
محمد واحديان شاه

Publication type:

Article

Euglycemic diabetic ketoacidosis caused by empagliflozin complicated by failure to thrive in a geriatric patient.

Published in:

2023

By:

Rathore, Azeem;
Gupta, Nidhi;
Kahn, Cameron;
Kadariya, Dinesh

Publication type:

Case Study

Pituitary hypoplasia and growth hormone deficiency in a patient with Coffin-Siris syndrome and severe short stature: case report and literature review.

Published in:

2022

By:

Bilha, Stefana Catalina;
Teodoriu, Laura;
Velicescu, Cristian;
Caba, Lavinia

Publication type:

Case Study

Modified Le Fort I Osteotomy and Genioplasty for Management of Severe Dentofacial Deformity in β-Thalassaemia Major: Case report and review of the literature.

Published in:

Sultan Qaboos University Medical Journal, 2020, v. 20, n. 3, p. e362, doi. 10.18295/squmj.2020.20.03.018

By:

Al Hasani, Khamis M.;
Bakathir, Abdulaziz A.;
Al-Hashmi, Ahmed K.;
Rawahi, Badar Al;
Albakri, Abdullah

Publication type:

Article

Resolution of high aortic valve systolic gradient suggesting significant stenosis following closure of patent ductus arteriosus.

Published in:

2024

By:

Mukhtar, Gousia;
Gopalakrishnan, Arun;
Krishnamoorthy, Kavassery Mahadevan

Publication type:

Case Study

Nasljedna nepodnošljivost fruktoze - pregled literature i prikaz dvoje bolesnika.

Published in:

Paediatria Croatica, 2021, v. 65, n. 1, p. 36, doi. 10.13112/pc.397

By:

Paponja, Kristina;
Rahelić, Valentina;
Mesarić, Nikola;
Žigman, Tamara;
Škaričić, Ana;
Bilandžija-Kuš, Iva;
Pavić, Eva;
Senečić-Čala, Irena;
Peršić, Mladen;
Vuković, Jurica;
Barić, Ivo;
Ramadža, Danijela Petković

Publication type:

Article

Incidental COVID‐19 in a heart‐kidney transplant recipient with malnutrition and recurrent infections: Implications for the SARS‐CoV‐2 immune response.

Published in:

Transplant Infectious Disease, 2020, v. 22, n. 6, p. 1, doi. 10.1111/tid.13367

By:

Serrano, Oscar K.;
Kutzler, Heather L.;
Rochon, Caroline;
Radojevic, Joseph A.;
Lawlor, Michael T.;
Hammond, Jonathan A.;
Gluck, Jason;
Feingold, Andrew D.;
Jaiswal, Abhishek

Publication type:

Article

Prevalence of Failure to Thrive and Associated Risk Factors in In-patients Under 5 Years of Age.

Published in:

Zahedan Journal of Research in Medical Sciences, 2023, v. 25, n. 3, p. 1, doi. 10.5812/zjrms-121896

By:

Khalili, Manijeh;
Teimouri, Alireza;
Babaeian, Masroor

Publication type:

Article

Severe labile hypertension in a patient with catecholamine-secreting neuroblastoma: a case report.

Published in:

Pediatric Nephrology, 2024, v. 39, n. 7, p. 2087, doi. 10.1007/s00467-023-06269-2

By:

Frisby-Zedan, Jeanne;
Migotsky, Michael;
Walterhouse, David O.;
Verghese, Priya S.

Publication type:

Article

Correction: A child with chronic kidney disease and hepatic dysfunction: Questions.

Published in:

2023

By:

Sethi, Sidharth Kumar;
Mohan, Neelam;
Rana, Alka;
Bagoria, Gaurav;
Soni, Kritika;
Sharma, Vivek;
Nair, Aishwarya;
Savita, Savita;
Bansal, Shyam Bihari;
Raina, Rupesh

Publication type:

Correction Notice

A child with chronic kidney disease and hepatic dysfunction: Questions.

Published in:

Pediatric Nephrology, 2023, v. 38, n. 10, p. 3275, doi. 10.1007/s00467-023-05924-y

By:

Sethi, Sidharth Kumar;
Mohan, Neelam;
Rana, Alka;
Bagoria, Gaurav;
Soni, Kritika;
Sharma, Vivek;
Nair, Aishwarya;
Savita, Savita;
Bansal, Shyam Bihari;
Raina, Rupesh

Publication type:

Article

Failure to thrive in an 8-month-old female: Answers.

Published in:

Pediatric Nephrology, 2023, v. 38, n. 7, p. 2079, doi. 10.1007/s00467-022-05788-8

By:

Kim, Romina;
Ye, XinYi;
Sanchez-Lara, Pedro A.;
Puliyanda, Dechu;
Kumar, Sanjeev;
Pizzo, Helen

Publication type:

Article

Failure to thrive in an 8-month-old female: Questions.

Published in:

Pediatric Nephrology, 2023, v. 38, n. 7, p. 2077, doi. 10.1007/s00467-022-05778-w

By:

Kim, Romina;
Ye, XinYi;
Sanchez-Lara, Pedro A.;
Puliyanda, Dechu;
Kumar, Sanjeev;
Pizzo, Helen

Publication type:

Article

Late-onset hypertension in a child with growth retardation: Questions.

Published in:

Pediatric Nephrology, 2022, v. 37, n. 10, p. 2337, doi. 10.1007/s00467-022-05491-8

By:

Leventoğlu, Emre;
Döğer, Esra;
Büyükkaragöz, Bahar;
Nalçacı, Sinem;
Öner, Ganimet;
Alpman, Bedriye Nuray;
Fidan, Kibriya;
Söylemezoğlu, Oğuz;
Bakkaloğlu, Sevcan A.

Publication type:

Article

Chediak Higashi syndrome with acute kidney injury: Questions.

Published in:

2022

By:

Kalra, Suprita;
Khera, Sanjeev;
Sharma, Aditi;
Daryani, Hitesh;
Singh, Vikram

Publication type:

Question & Answer

Pseudo-Bartter syndrome and staghorn calculi in an infant with chronic diarrhea: Questions.

Published in:

2021

By:

Leventoğlu, Emre;
Büyükkaragöz, Bahar;
Düztaş, Demet Teker;
Gürkan, Ödül Eğritaş

Publication type:

Case Study

A hypertensive girl with failure to thrive accompanied by gastrointestinal symptoms: Answers.

Published in:

2021

By:

Selcuk, Senay Zirhli;
Elmas, Ahmet Taner;
Yildirim, Ismail Okan;
Sigirci, Ahmet;
Sozeri, Betul;
Tabel, Yılmaz

Publication type:

Test/Instrument

A hypertensive girl with failure to thrive accompanied by gastrointestinal symptoms: Questions.

Published in:

2021

By:

Selcuk, Senay Zirhli;
Elmas, Ahmet Taner;
Yildirim, Ismail Okan;
Sigirci, Ahmet;
Sozeri, Betul;
Tabel, Yilmaz

Publication type:

Test/Instrument

When salt is needed to grow: Questions.

Published in:

2021

By:

Conversano, Ester;
Romano, Sara;
Taddio, Andrea;
Faletra, Flavio;
Zanon, Davide;
Barbi, Egidio;
Pennesi, Marco

Publication type:

Question & Answer

A rare cause of chronic hyponatremia in an infant: Answers.

Published in:

Pediatric Nephrology, 2020, v. 35, n. 2, p. 243, doi. 10.1007/s00467-019-04337-0

By:

Mutlu, Gül Yeşiltepe;
Taşdemir, Mehmet;
Kızılkan, Nuray Uslu;
Güran, Tülay;
Hatun, Şükrü;
Kayserili, Hülya;
Bilge, Ilmay

Publication type:

Article

A rare cause of chronic hyponatremia in an infant: Questions.

Published in:

2020

By:

Mutlu, Gül Yeşiltepe;
Taşdemir, Mehmet;
Kızılkan, Nuray Uslu;
Güran, Tülay;
Hatun, Şükrü;
Kayserili, Hülya;
Bilge, Ilmay

Publication type:

Case Study

A rare cause of hypertension in childhood: Questions.

Published in:

2020

By:

Kucuk, Nuran;
Yavas Abali, Zehra;
Abali, Saygın;
Canpolat, Nur;
Yesil, Gozde;
Turan, Serap;
Bereket, Abdullah;
Guran, Tulay

Publication type:

Case Study

Uncommon cribfellows: an infant with hypercalcemia, nephrocalcinosis, and acidosis: Questions.

Published in:

Pediatric Nephrology, 2018, v. 33, n. 10, p. 1695, doi. 10.1007/s00467-018-3887-5

By:

Ehlayel, Abdulla M.;
Copelovitch, Lawrence

Publication type:

Article

Vomiting in an infant with congenital nephrotic syndrome: Questions.

Published in:

Pediatric Nephrology, 2017, v. 32, n. 9, p. 1519, doi. 10.1007/s00467-016-3529-8

By:

Takahashi, Toshiyuki;
Sato, Yasuyuki;
Yamazaki, Takeshi;
Hayashi, Asako;
Okamoto, Takayuki

Publication type:

Article

A neonate with poor weight gain and hyperkalemia: Questions.

Published in:

Pediatric Nephrology, 2017, v. 32, n. 1, p. 71, doi. 10.1007/s00467-015-3280-6

By:

Liu, Chiung-Chen;
Lin, Shih-Hua;
Sung, Chih-Chien;
Lin, Chien-Ming

Publication type:

Article

Fibroblast growth factor-23 and renin-angiotensin system levels in vitamin-D-dependent rickets type I.

Published in:

Pediatric Nephrology, 2016, v. 31, n. 7, p. 1189, doi. 10.1007/s00467-016-3356-y

By:

Cuervo, Carlos;
Abitbol, Carolyn;
Zilleruelo, Gaston;
Freundlich, Michael

Publication type:

Article

Maternal and infantile hypercalcemia caused by vitamin-D-hydroxylase mutations and vitamin D intake.

Published in:

Pediatric Nephrology, 2015, v. 30, n. 1, p. 145, doi. 10.1007/s00467-014-2889-1

By:

Dinour, Dganit;
Davidovits, Miriam;
Aviner, Shraga;
Ganon, Liat;
Michael, Leonid;
Modan-Moses, Dalit;
Vered, Iris;
Bibi, Haim;
Frishberg, Yaacov;
Holtzman, Eli

Publication type:

Article

Protein-energy wasting and uremic failure to thrive in children with chronic kidney disease: They are not small adults.

Published in:

2014

By:

Nourbakhsh, Noureddin;
Rhee, Connie;
Kalantar-Zadeh, Kamyar

Publication type:

Editorial

An unusual cause of severe rickets: Questions.

Published in:

Pediatric Nephrology, 2014, v. 29, n. 3, p. 387, doi. 10.1007/s00467-013-2516-6

By:

Jahan, Afsana;
Agarwal, Indira;
Chaturvedi, Swasti

Publication type:

Article

An unusual cause of severe rickets: Answers.

Published in:

Pediatric Nephrology, 2014, v. 29, n. 3, p. 389, doi. 10.1007/s00467-013-2522-8

By:

Jahan, Afsana;
Agarwal, Indira;
Chaturvedi, Swasti

Publication type:

Article

Mitochondrial tRNA mutation as a cause of end-stage renal disease in childhood.

Published in:

2013

By:

D'Aco, Kristin;
Manno, Megan;
Clarke, Colleen;
Ganesh, Jaya;
Meyers, Kevin;
Sondheimer, Neal

Publication type:

Report

Bartter syndrome and growth hormone deficiency: three cases.

Published in:

2012

By:

Buyukcelik, Mithat;
Keskin, Mehmet;
Kilic, Beltinge;
Kor, Yilmaz;
Balat, Ayse

Publication type:

Report

Neonatal atypical hemolytic uremic syndrome due to methylmalonic aciduria and homocystinuria.

Published in:

2012

By:

Menni, Francesca;
Testa, Sara;
Guez, Sophie;
Chiarelli, Gabriella;
Alberti, Luisella;
Esposito, Susanna

Publication type:

Report

Infantile midaortic syndrome with aortic occlusion.

Published in:

2012

By:

Minson, Susan;
McLaren, Clare;
Roebuck, Derek;
Tullus, Kjell

Publication type:

Report

An infant with alternating metabolic acidosis and alkalosis: answer.

Published in:

Pediatric Nephrology, 2012, v. 27, n. 1, p. 53, doi. 10.1007/s00467-011-1901-2

By:

Hooman, Nakysa;
Jafari, Daniel;
Jalali-Farahani, Sahar;
Lahouti Harahdashti, Arash

Publication type:

Article

Failure to thrive and nephrolithiasis in a boy with congenital cyanotic heart anomaly-questions.

Published in:

Pediatric Nephrology, 2011, v. 26, n. 12, p. 2153, doi. 10.1007/s00467-011-1786-0

By:

Tasic, Velibor;
Lozanovski, Vladimir;
Gucev, Zoran;
Blau, Nenad;
Cheong, Hae;
Sayer, John

Publication type:

Article