Works matching DE "DEVELOPMENTAL delay"

Results: 2352

Neurodevelopmental Status of Children Born During COVID-19 Pandemic in Belagavi City: A Cross-Sectional Study.

Published in:

National Journal of Community Medicine, 2025, v. 16, n. 5, p. 501, doi. 10.55489/njcm.160520254860

By:

Kalgutkar, Pratiksha;
Deshpande, Vinuta

Publication type:

Article

Senior–Loken Syndrome: Ocular Perspectives on Genetics, Pathogenesis, and Management.

Published in:

Biomolecules (2218-273X), 2025, v. 15, n. 5, p. 667, doi. 10.3390/biom15050667

By:

Zhou, Di;
Zeng, Yi;
Luo, Weihan;
Leng, Chenyang;
Li, Chen

Publication type:

Article

The Homeobox Transcription Factor CUX1 Coordinates Postnatal Epithelial Developmental Timing but Is Dispensable for Lung Organogenesis and Regeneration.

Published in:

American Journal of Respiratory Cell & Molecular Biology, 2025, v. 72, n. 6, p. 678, doi. 10.1165/rcmb.2024-0147OC

By:

Zhao, Barbara;
Socha, Jacob;
Toth, Andrea;
Fernandes, Sharlene;
Warheit-Niemi, Helen;
Ruff, Brandy;
Khurana Hershey, Gurjit K.;
VanDussen, Kelli L.;
Swarr, Daniel;
Zacharias, William J.

Publication type:

Article

Ears of the Lynx Sign in Lipoyl Transferase-2 (LIPT2) Deficiency.

Published in:

Neurology India, 2025, v. 73, n. 3, p. 634, doi. 10.4103/neurol-india.Neurol-India-D-24-00717

By:

Sharma, Yashu;
Gunasekaran, Pradeep Kumar;
Saini, Arushi Gahlot;
Bhatia, Vikas

Publication type:

Article

Report of Three Cases of Persistent Hypoglossal Artery with Associated Anomalies and a Review of Literature.

Published in:

2025

By:

Nagarajan, Krishnan;
Amuthabharathi, Mohan;
Adithan, Subathra;
Gowtham, Mahadevan S

Publication type:

Letter

Developmental perspectives on HiTOP psychosis superspectrum: Unveiling pitfalls and theoretical fallacies.

Published in:

Frontiers in Psychiatry, 2025, p. 1, doi. 10.3389/fpsyt.2025.1523025

By:

Poletti, Michele;
Preti, Antonio;
Raballo, Andrea

Publication type:

Article

Porencephalic Cysts and Siderosis in COL4A1 Mutation-Related Disorder.

Published in:

Neurology India, 2025, v. 73, n. 2, p. 400, doi. 10.4103/neurol-india.Neurol-India-D-24-00628

By:

Saini, Lokesh;
Gunasekaran, Pradeep Kumar;
Tiwari, Sarbesh;
Singh, Kuldeep

Publication type:

Article

VPS51 -Related Disorder in a Toddler: A Novel Golgipathy.

Published in:

Neurology India, 2025, v. 73, n. 2, p. 402, doi. 10.4103/neurol-india.Neurol-India-D-24-00743

By:

Bhanudeep, Singanamalla;
Koneti, Bramhini Bhargavi

Publication type:

Article

A Novel Genotype in Early Onset Atypical Absence Epilepsy.

Published in:

2025

By:

Koshy, Kiren G.;
Fasaludeen, Alfiya;
Menon, Ramshekhar N.

Publication type:

Letter

Congenital Hypothyroidism with Neuronal Migration Anomaly.

Published in:

Neurology India, 2024, v. 72, n. 2, p. 462, doi. 10.4103/neurol-india.Neurol-India-D-24-00195

By:

Maivizhi, Shruthi M.;
Sahoo, Biswajit;
Nayak, Manoj Kumar

Publication type:

Article

Chromosomal Duplication Syndromes: A Case Series.

Published in:

Neurology India, 2024, v. 72, n. 1, p. 124, doi. 10.4103/ni.ni_400_21

By:

Panigrahi, Inusha;
Shariq, Mohammed;
Bamba, Chitra;
Kaur, Ramandeep;
Bhatt, Yogita;
Srivastava, Priyanka

Publication type:

Article

Family Capacity-Building in Early Childhood Intervention: Do Context and Setting Matter?

Published in:

School Community Journal, 2014, v. 24, n. 1, p. 37

By:

Dunst, Carl J.;
Bruder, Mary Beth;
Espe-Sherwindt, Marilyn

Publication type:

Article

Facilitating Family Involvement in Early Intervention to Preschool Transition.

Published in:

School Community Journal, 2010, v. 20, n. 2, p. 183

By:

Yanhui Pang

Publication type:

Article

Racial Disparities in Preschool Special Education Eligibility for Five Southern States.

Published in:

Journal of Special Education, 2012, v. 46, n. 3, p. 152, doi. 10.1177/0022466910380465

By:

Morrier, Michael J.;
Gallagher, Peggy A.

Publication type:

Article

Ethnic Differences in Autism Eligibility in the United States Public Schools.

Published in:

Journal of Special Education, 2012, v. 46, n. 1, p. 49, doi. 10.1177/0022466910372137

By:

Morrier, Michael J.;
Hess, Kristen L.

Publication type:

Article

A high level of tetrasomy 9p mosaicism but no clinical manifestations other than moderate oligozoospermia with chromosomally balanced sperm: a case report.

Published in:

Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 3, p. 573, doi. 10.1007/s10815-020-01690-0

By:

Bellil, Hela;
Herve, Bérenice;
Herzog, Elodie;
Ayoubi, Jean-Marc;
Vialard, François;
Poulain, Marine

Publication type:

Article

Fertilization outcome, embryo development and birth after unstimulated IVM.

Published in:

Journal of Assisted Reproduction & Genetics, 2011, v. 28, n. 2, p. 107, doi. 10.1007/s10815-010-9490-8

By:

Bos-Mikich, Adriana;
Ferreira, Marcelo;
Höher, Marcos;
Frantz, Gerta;
Oliveira, Norma;
Dutra, Caroline;
Frantz, Nilo

Publication type:

Article

Can the Ages and Stages Questionnaire identify developmental delay?

Published in:

Practitioner, 2022, v. 266, n. 1862, p. 8

By:

SAUL, PETER

Publication type:

Article

Born Into Addiction: Neonatal Abstinence Syndrome and Pediatric Dentistry.

Published in:

Pediatric Dentistry, 2017, v. 39, n. 5, p. 358

By:

Cully, Jennifer L.

Publication type:

Article

Atypical presentation of Dyggve-Melchior-Clausen disease in a Moroccan child without developmental delay and intellectual disabilities.

Published in:

2024

By:

Elmakhzen, Badreddine;
Bouguenouch, Laila;
Oussama, Kettani;
Ali el asri, Yasser;
Askander, Omar

Publication type:

Case Study

Identification of the synonymous variant c.3141G > A in TNRC6B gene that altered RNA splicing by minigene assay.

Published in:

Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09835-5

By:

Zhou, Feiyu;
Zhong, Hongping;
Wu, Bo;
Cui, Yaqiong;
Li, Jiaci;
Jia, Xiaodong;
Yu, Changshun;
Li, Dong;
Shu, Jianbo;
Cai, Chunquan

Publication type:

Article

The Association Between Congenital Heart Disease and Autism Spectrum Disorder: A Systematic Review and Meta-Analysis.

Published in:

Pediatric Cardiology, 2023, v. 44, n. 5, p. 1092, doi. 10.1007/s00246-023-03146-5

By:

Gu, Sophia;
Katyal, Abhay;
Zhang, Qian;
Chung, Winnie;
Franciosi, Sonia;
Sanatani, Shubhayan

Publication type:

Article

Examining the ecology of preschool inclusion in New York City: A mixed-methods study underway.

Published in:

Contemporary Issues in Early Childhood, 2024, v. 25, n. 4, p. 503, doi. 10.1177/14639491241229229

By:

Gupta, Sarika S.;
Cheatham, Gregory A;
Strassfeld, Natasha;
Zhu, Xiaohan;
Medellin, Cristina;
Nagasawa, Mark

Publication type:

Article

Marinesco-Sjögren Syndrome in an Emirati Child with a Novel Mutation in SIL1 Affecting the 5' Untranslated Region.

Published in:

2016

By:

Nair, Pratibha;
Hamzeh, abdul Rezzak;
Mohamed, Madiha;
Tawfiq, Nafisa;
al-ali, Mahmoud Taleb;
Bastaki, Fatma

Publication type:

journal article

Assessment of motor development in children with postural asymmetry and the application of neurodevelopmental-based improvement methods.

Published in:

Rheumatology Forum, 2024, v. 10, n. 4, p. 194, doi. 10.5603/rf.90800

By:

Malak, Roksana;
Torzyńska, Patrycja;
Żółkiewska, Joanna;
Matecka, Monika;
Samborski, Włodzimierz

Publication type:

Article

Comparison Between The Impact Of TPN With Laminar Flow And Without Laminar Flow On Outcomes Of Neonatal Intensive Care Units In Zagazig University Children's Hospital.

Published in:

Zagazig University Medical Journal, 2023, v. 29, p. 314, doi. 10.21608/ZUMJ.2021.53142.2042

By:

El-banna, Ehab Abdelmonem;
Anany, Heba Gamal;
Mohamed, Aya Ismail Kotb

Publication type:

Article

SPEECH DELAY AND EXCESSIVE GADGET USAGE: UNDERSTANDING PATHOPHYSIOLOGY MECHANISM AND PREVENTION TARGET AMONG CHILDREN POPULATION.

Published in:

Eduvest: Journal Of Universal Studies, 2024, v. 4, n. 9, p. 7932, doi. 10.59188/eduvest.v4i9.1265

By:

Sindhutomo, Jopi Chandra

Publication type:

Article

Hypocalcemia -- a Diagnostic Challenge.

Published in:

Central European Journal of Paediatrics, 2023, v. 19, n. 1, p. 50, doi. 10.5457/p2005-114.337

By:

Gomes, Mariana Bastos;
Azevedo, André Costa;
Marinhas, Andreia;
Costa, Mariana;
Carneiro, Ana Catarina;
Figueiredo, Suzana

Publication type:

Article

Supporting Parents of Children with Intellectual Disabilities in a Special Needs Class in Gauteng, South Africa.

Published in:

African Journal of Development Studies, 2023, v. 13, p. 273, doi. 10.31920/2634-3649/2023/sin1a14

By:

Le Roux, Vanessa Margaret;
Fourie, Jean Veronica

Publication type:

Article

Screening for Developmental Delays in Children 2-36 Months of Age in a Primary Health Care Center in Cairo, Egypt.

Published in:

Journal of High Institute of Public Health, 2022, v. 52, n. 2, p. 53, doi. 10.21608/jhiph.2022.254505

By:

Abdelbaky, Omnya A.;
Deifallah, Shaymaa;
Amin, Ghada;
Marzouk, Diaa

Publication type:

Article

Prevalence and Factors Associated with Developmental Delays among Preschool Children in Saudi Arabia.

Published in:

Journal of High Institute of Public Health, 2020, v. 50, n. 1, p. 10, doi. 10.21608/jhiph.2020.79318

By:

Shatla, Mokhtar M.;
Goweda, Reda A.

Publication type:

Article

A de novo microdeletion 2p24.3-25.1 identified in a girl with global development delay.

Published in:

BioDiscovery, 2017, p. 1, doi. 10.7750/BioDiscovery.2015.18.1

By:

Ivanov, Hristo Y.;
Stoyanova, Vili K.;
Vazharova, Radoslava;
Linev, Aleksandar;
Ivanov, Ivan;
Ivanov, Samuil;
Balabanski, Lubomir;
Toncheva, Draga

Publication type:

Article

An evaluation of the effectiveness of a therapeutic program for children with global developmental delay.

Published in:

Arab Gulf Journal of Scientific Research, 2023, v. 41, n. 4, p. 627, doi. 10.1108/AGJSR-09-2022-0195

By:

Al-Yamani, Abyan Ismail;
Sulaiman, Nabil Ali;
Al-Ansari, Ahmed Malalla

Publication type:

Article

Effectiveness of a Multimodal Intervention using Movement, Mental Exercise and Dietary Approaches on Children with Specific Learning Difficulties.

Published in:

Asia Pacific Journal of Developmental Differences, 2021, v. 8, n. 1, p. 31, doi. 10.3850/S2345734121000022

By:

Huan, Isaac Tan Chiang;
Lim Zhong Hao;
Joyce Ang Yan Ting

Publication type:

Article

ATP1A3-Associated Paroxysmal Dystonia.

Published in:

2024

By:

Ledoux, Mark S.

Publication type:

Case Study

Tremor-Dominant Movement Disorder in ANKRD11- Associated KBG Syndrome.

Published in:

Tremor & Other Hyperkinetic Movements, 2024, v. 14, n. 1, p. 1, doi. 10.5334/tohm.926

By:

Stehr, Antonia M.;
Koeglsperger, Thomas;
Jacob, Maureen;
Rhodio, Valerio;
Winkelmann, Juliane;
Hopfner, Franziska;
Zech, Michael

Publication type:

Article

Disease genetics: Searching large and small.

Published in:

Nature Reviews Genetics, 2014, v. 15, n. 11, p. 706, doi. 10.1038/nrg3840

By:

Lau, Esther

Publication type:

Article

The TANGO2 disease and the therapeutic challenge of acute arrhythmia management: a case report.

Published in:

European Heart Journal Case Reports, 2023, v. 7, n. 2, p. 1, doi. 10.1093/ehjcr/ytad044

By:

Gomes, Sílvia A;
Laranjo, Sérgio;
Trigo, Conceição;
Pinto, Fátima F

Publication type:

Article

EXPERIENCIAS DE APEGO EN MADRES DE NIÑOS CON RETRASO MADURATIVO: ANÁLISIS DE CONTENIDO.

Published in:

Siglo Cero, 2020, v. 51, n. 1, p. 89, doi. 10.14201/scero202051189109

By:

GARCÍA TORO, Maritza;
SÁNCHEZ GÓMEZ, Maria Cruz

Publication type:

Article

Comparing the effects and potencies of perchlorate and nitrate on amphibian metamorphosis using a modified amphibian metamorphosis assay (AMA).

Published in:

Journal of Applied Toxicology, 2024, v. 44, n. 8, p. 1184, doi. 10.1002/jat.4611

By:

Fort, Douglas J.;
Peake, Brittanie F.;
Mathis, Michael B.;
Leopold, M. Annegaaike;
Wolf, Jeffrey C.;
Weterings, Peter J. J. M.

Publication type:

Article

Influence of systemic copper toxicity on early development and metamorphosis in Xenopus laevis.

Published in:

Journal of Applied Toxicology, 2023, v. 43, n. 3, p. 431, doi. 10.1002/jat.4393

By:

Fort, Douglas J.;
Todhunter, Kevin J.;
Wolf, Jeffrey C.;
Long, Kevin;
Poland, Craig A.;
McGrath, Micheal;
Baken, Stijn;
Mackie, Carol

Publication type:

Article

School Teachers’ Teaching Experience on Self-efficacy and Life Satisfaction.

Published in:

Indian Journal of Community Psychology, 2017, v. 13, n. 1, p. 190

By:

Basak, Rituparna

Publication type:

Article

Identification and Characterization of New Variants in FOXRED1 Gene Expands the Clinical Spectrum Associated with Mitochondrial Complex I Deficiency.

Published in:

Journal of Clinical Medicine, 2019, v. 8, n. 8, p. 1262, doi. 10.3390/jcm8081262

By:

Barbosa-Gouveia, Sofia;
González-Vioque, Emiliano;
Borges, Filipa;
Gutiérrez-Solana, Luis;
Wintjes, Liesbeth;
Kappen, Antonia;
van den Heuvel, Lambert;
Leis, Rosaura;
Rodenburg, Richard;
Couce, María Luz

Publication type:

Article

Early Clinical Predictors of Autism Spectrum Disorder in Infants with Tuberous Sclerosis Complex: Results from the EPISTOP Study.

Published in:

Journal of Clinical Medicine, 2019, v. 8, n. 6, p. 788, doi. 10.3390/jcm8060788

By:

Moavero, Romina;
Benvenuto, Arianna;
Emberti Gialloreti, Leonardo;
Siracusano, Martina;
Kotulska, Katarzyna;
Weschke, Bernhard;
Riney, Kate;
Jansen, Floor E.;
Feucht, Martha;
Krsek, Pavel;
Nabbout, Rima;
Jansen, Anna C.;
Wojdan, Konrad;
Borkowska, Julita;
Sadowski, Krzystof;
Hertzberg, Christoph;
Hulshof, Hanna;
Samueli, Sharon;
Benova, Barbora;
Aronica, Eleonora

Publication type:

Article

A Case of Rafiq Syndrome (MAN1B1-CDG) in a Palestinian Child, With Brief Literature Review of 44 Cases.

Published in:

Journal of Investigative Medicine High Impact Case Reports, 2025, p. 1, doi. 10.1177/23247096251313731

By:

Iskafi, Reema;
AbuRahmeh, Bahaa;
Aljuneidi, Roa'a;
AlShweiki, Hidaya;
Abdelnabi, Siraj;
Abukhalaf, Anas;
Maraqa, Bara'

Publication type:

Article

An expansion of phenotype: novel homozygous variant in the MED17 identified in patients with progressive microcephaly and global developmental delay.

Published in:

Journal of Neurogenetics, 2022, v. 36, n. 4, p. 108, doi. 10.1080/01677063.2022.2149748

By:

Rafiullah, Rafiullah;
Albalawi, Alia M.;
Alaradi, Sultan R.;
Alluqmani, Majed;
Mushtaq, Muhammad;
Wali, Abdul;
Basit, Sulman

Publication type:

Article

De novo mutation in SLC25A22 gene: expansion of the clinical and electroencephalographic phenotype.

Published in:

Journal of Neurogenetics, 2021, v. 35, n. 2, p. 67, doi. 10.1080/01677063.2021.1892094

By:

Nicotera, Antonio Gennaro;
Dicanio, Daniela;
Pironti, Erica;
Bonsignore, Maria;
Cafeo, Anna;
Efthymiou, Stephanie;
Mondello, Patrizia;
Salpietro, Vincenzo;
Houlden, Henry;
Di Rosa, Gabriella

Publication type:

Article

Novel mutation in the <italic>KCNJ10</italic> gene in three siblings with seizures, ataxia and no electrolyte abnormalities.

Published in:

Journal of Neurogenetics, 2018, v. 32, n. 1, p. 1, doi. 10.1080/01677063.2017.1404057

By:

Al Dhaibani, Muna A.;
El-Hattab, Ayman W.;
Holroyd, Kathryn B.;
Orthmann-Murphy, Jennifer;
Larson, Valerie A.;
Siddiqui, Khurram A.;
Szolics, Miklos;
Schiess, Nicoline

Publication type:

Article

Silent victims of the COVID-19 pandemic may be infants who are at a risk of a neurodevelopmental delay: a cross-sectional study.

Published in:

Early Child Development & Care, 2024, v. 194, n. 15/16, p. 1485, doi. 10.1080/03004430.2024.2424188

By:

Erol, Gökçen;
Arman, Nilay

Publication type:

Article

Positive and multifaceted perceptions of Israeli kindergarten teachers contribute to developmental gains of children with developmental delay.

Published in:

Early Child Development & Care, 2024, v. 194, n. 5/6, p. 769, doi. 10.1080/03004430.2024.2341732

By:

Sher-Censor, Efrat;
Dolev, Smadar;
Shalem Gan-Or, Michal;
Zach, Esther

Publication type:

Article