Search Results - "Al-Mamari, Watfa"

Applying Whole Exome Sequencing in a Consanguineous Population with Autism Spectrum Disorder

Authors: Al-Mamari, Watfa Idris, Ahmed B. Al-Thihli, Khalid et al.

Source: International Journal of Developmental Disabilities. 2023 69(2):190-200.

Peer Reviewed: Y

Page Count: 11

Descriptors: Autism Spectrum Disorders, Genetics, Children, Etiology, Clinical Diagnosis, Symptoms (Individual Disorders)

A 'SWOT' Analysis of Parent-Mediated Intervention for Children with Autism Spectrum Disorder: Oman as a Regional Model

Authors: Idris, Ahmed B. Abdulrahim, Reem Al-Mamari, Watfa et al.

Source: International Journal of Developmental Disabilities. 2022 68(5):773-780.

Peer Reviewed: Y

Page Count: 8

Descriptors: Foreign Countries, Autism Spectrum Disorders, Children, Intervention, Parent Role, Strategic Planning, Program Effectiveness

Geographic Terms: Oman

Shaping Oman’s Child Health Future by 2040: Key projections for population and workforce in developmental-behavioural paediatrics.

Authors: Al-Mamari, Watfa Idris, Ahmed B. Al-Balushi, Rola et al.

Source: Sultan Qaboos University Medical Journal. 2025, Vol. 25 Issue 1, p1129-1134. 6p. 1 Chart, 1 Map.

Nurturing the Future: Understanding maternal knowledge of child development in Oman.

Authors: Al-Mamari, Watfa Idris, Ahmed B. Jalees, Saquib et al.

Source: Sultan Qaboos University Medical Journal. 2025, Vol. 25 Issue 1, p352-362. 11p.

Consanguinity: The innocent culprit in autism severity.

Authors: Al-Mamari, Watfa Idris, Ahmed B. Fadlallah, Najat et al.

Source: Sultan Qaboos University Medical Journal. 2025, Vol. 25 Issue 1, p114-121. 8p.

Perception about telemedicine services among parents of children with neurodevelopmental disorders in a specialised tertiary centre in Oman.

Authors: B. Idris, Ahmed Al-Mamari, Watfa Al Humaidi, Taif Saud et al.

Source: Global Public Health. Jan2024, Vol. 19 Issue 1, p1-12. 12p.

Enhancing Child Development in Oman: Applying global agenda into local context.

Authors: Al-Mamari, Watfa Idris, Ahmed B. Al-Alawi, Kamila et al.

Source: Sultan Qaboos University Medical Journal. May2023, Vol. 23 Issue 2, p143-147. 5p.

Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of Patients with Autism Spectrum Disorders from a Highly Consanguineous Population

Authors: Al-Mamari, Watfa Al-Saegh, Abeer Al-Kindy, Adila et al.

Source: Journal of Autism and Developmental Disorders. Aug 2015 45(8):2323-2328.

Peer Reviewed: Y

Page Count: 6

Descriptors: Autism, Pervasive Developmental Disorders, Children, Genetic Disorders, Genetics, Foreign Countries

Geographic Terms: Oman

Parental Age and the Risk of Autism Spectrum Disorder in Oma.

Authors: Al-Mamari, Watfa Idris, Ahmed B. Al-Zadjali, Aala' A. et al.

Source: Sultan Qaboos University Medical Journal. Aug2021, Vol. 21 Issue 3, p465-471. 7p.

Intellectual Profile of Children with Autism Spectrum Disorder.

Authors: Al-Mamari, Watfa Idris, Ahmed B. Gabr, Ahlam et al.

Source: Sultan Qaboos University Medical Journal. Aug2021, Vol. 21 Issue 3, p386-393. 8p.

Could a National Screening Program Reduce the Age of Diagnosis of Autism Spectrum Disorder?

Authors: Al-Mamari, Watfa Idris, Ahmed B. Al Aamri, Hafsa et al.

Source: Journal of Autism & Developmental Disorders. Feb2025, p1-15.

Comorbidity of Learning Disorders and Attention Deficit Hyperactivity Disorder in a Sample of Omani Schoolchildren.

Alternate Title: التلازم بين اضطرابات التعلم واضطراب نقص الانتباه المصاحب بالحركة الزائدة في عينة من تلاميذ المدارس في سلطنة عمان

Authors: Al-Mamari, Watfa S. Emam, Mahmoud M. Al-Futaisi, Amna M. et al.

Source: Sultan Qaboos University Medical Journal. Nov2015, Vol. 15 Issue 4, p528-533. 6p.

De Novo Duplication of 7p21.1p22.2 in a Child with Autism Spectrum Disorder and Craniofacial Dysmorphism.

Alternate Title: وجود طفرة جينية للتضاعف الصبغي في 7p21. 1p22.2 في طفل لديه اضطراب طيف التوحد واختلافات خلقية

Authors: Udayakumar, Achandira M. Al-Mamari, Watfa Al-Sayegh, Abeer et al.

Source: Sultan Qaboos University Medical Journal. Aug2015, Vol. 15 Issue 3, pe415-e419. 5p.

Further phenotypic delineation of Alazami syndrome.

Authors: Al‐Hinai, Abdulhamid Al‐Hashmi, Samiya Ganesh, Anuradha et al.

Source: American Journal of Medical Genetics. Part A; Aug2022, Vol. 188 Issue 8, p2485-2490, 6p

Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family.

Authors: Al‐Amri, Ahmed Saegh, Abeer Al Al‐Mamari, Watfa et al.

Source: American Journal of Medical Genetics. Part A; Jul2016, Vol. 170A Issue 7, p1826-1831, 6p

A Turning Point for Paediatric Developmental Services in Oman.

Authors: Al-Mamari, Watfa Idris, Ahmed B. Al-Jabri, Muna et al.

Source: Sultan Qaboos University Medical Journal. Feb2017, Vol. 17 Issue 1, pe125-e126. 2p.

Genetic Variant Analyses Identify Novel Candidate Autism Risk Genes from a Highly Consanguineous Cohort of 104 Families from Oman.

Authors: Gupta, Vijay Ben-Mahmoud, Afif Idris, Ahmed B. et al.

Source: International Journal of Molecular Sciences. Dec2024, Vol. 25 Issue 24, p13700. 24p.

Expanding the clinical spectrum of cytosolic phosphoenolpyruvate carboxykinase deficiency: novel PCK1 variants in four Arabian Gulf families.

Authors: Al Busaidi, Marwa Mohamed, Feda E. Al-Ajmi, Eiman et al.

Source: Orphanet Journal of Rare Diseases. 11/3/2023, Vol. 18 Issue 1, p1-10. 10p.

Learning Disabilities.

Alternate Title: صعوبات التعلم.

Authors: Al-Mahrezi, Abdulaziz Al-Futaisi, Amna Al-Mamari, Watfa

Source: Sultan Qaboos University Medical Journal. May2016, Vol. 16 Issue 2, p129-131. 3p.

The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families.

Authors: Al-Kasbi, Ghalia Al-Murshedi, Fathiya Al-Kindi, Adila et al.

Source: Scientific Reports. 11/7/2022, Vol. 12 Issue 1, p1-12. 12p.