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Brief Report: First Identification of Intrafamilial Recurrence of Blau Syndrome due to Gonosomal NOD2 Mosaicism

Arthritis & rheumatology (Hoboken, N.J.), 2016-04, Vol.68 (4), p.1039-1044

2016

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Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia

Journal of dermatological science, 2015-04, Vol.78 (1), p.82-85

2015

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A case of TREM2 mutation presenting with features of progressive non-fluent aphasia and without bone involvement

Australian and New Zealand journal of psychiatry, 2017-11, Vol.51 (11), p.1157-1158

2017

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The Perceived Attributes of EMA and its Relation to the Adoption of the Practice: Malaysian Evidence

International journal of recent technology and engineering, 2020-03, Vol.8 (6), p.3186-3189

Ariffin, Avylin Roziana Mohd

2020

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A case of early-onset familial Alzheimer’s disease with both APP and novel PSEN2 mutations presenting with non-amnestic features

Australian and New Zealand journal of psychiatry, 2017-12, Vol.51 (12), p.1252-1253

2017

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Outcomes of Patients with EGFR-Mutant Advanced NSCLC in a Developing Country in Southeast Asia

Cancer management and research, 2022-06, Vol.14, p.1995-2005

2022

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Guidelines on retention of pathology records and materials (Version 2/2022)

Malaysian journal of pathology, 2022-08, Vol.44 (2), p.165-176

2022

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Mutation and pathogenic study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia

Journal of dermatological science, 2016-10, Vol.84 (1), p.e48-e48

2016

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Corrigendum to ‘Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia’ [Journal of Dermatological Science 78 (2015) 82–85]

Journal of dermatological science, 2015-08, Vol.79 (2), p.179-180

2015

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Financial Inclusion through Islamic Finance: Measurement Framework

The journal of muamalat and Islamic finance research : JMIFR, 2017-12, Vol.14 (2), p.129-155

2017

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CONSEQUENCES OF ENVIRONMENTAL MANAGEMENT ACCOUNTING (EMA): THE THEORY BEHIND

International journal of business and applied social science, 2020-11, p.20-27

Mohd Ariffin, Dr. Avylin Roziana

2020

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A case of TREM2 mutation presenting with features of progressive non-fluent aphasia and without bone involvement

The Australian and New Zealand journal of psychiatry, 2017, Vol.51 (11), p.1157-1158

2017

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A case of early-onset familial Alzheimer's disease with both APP and novel PSEN2 mutations presenting with non-amnestic features

The Australian and New Zealand journal of psychiatry, 2017, Vol.51 (12), p.1252-1253

2017

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Brief Report: First Identification of Intrafamilial Recurrence of Blau Syndrome due to Gonosomal NOD2 Mosaicism

Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia

A case of TREM2 mutation presenting with features of progressive non-fluent aphasia and without bone involvement

The Perceived Attributes of EMA and its Relation to the Adoption of the Practice: Malaysian Evidence

A case of early-onset familial Alzheimer’s disease with both APP and novel PSEN2 mutations presenting with non-amnestic features

Outcomes of Patients with EGFR-Mutant Advanced NSCLC in a Developing Country in Southeast Asia

Guidelines on retention of pathology records and materials (Version 2/2022)

Mutation and pathogenic study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia

Corrigendum to ‘Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia’ [Journal of Dermatological Science 78 (2015) 82–85]

Financial Inclusion through Islamic Finance: Measurement Framework

CONSEQUENCES OF ENVIRONMENTAL MANAGEMENT ACCOUNTING (EMA): THE THEORY BEHIND

A case of TREM2 mutation presenting with features of progressive non-fluent aphasia and without bone involvement

A case of early-onset familial Alzheimer's disease with both APP and novel PSEN2 mutations presenting with non-amnestic features

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