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FERDY KURNIAWAN CAYAMI

Assistant Professor

Bachelor Program of Medicine

Medical Faculty


Publications

Dr. Ferdy Kurniawan Cayami, M.Si.Med

Biography

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Mechanical stress regulates bone regulatory gene expression independent of estrogen and vitamin D deficiency in rats

Q1

JOURNAL OF ORTHOPAEDIC RESEARCH (ISSN: 07360266) , vol. 39 , pp. 42-52

Creator: Nepal A.K.

2021

3 cited

Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C

Q1

JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM (ISSN: 0021972X) , vol. 106 , pp. E660-E674

Creator: Pelletier F.

2021

11 cited

Attitudes of Indonesian health science undergraduates toward sexuality in individuals with intellectual disabilities

Q1

RESEARCH IN DEVELOPMENTAL DISABILITIES (ISSN: 08914222) , vol. 118

Creator: Evlyn D.

2021

0 cited

Familiarity and genetic literacy among medical students in Indonesia

Q1

BMC MEDICAL EDUCATION , vol. 21

Creator: Swandayani Y.M.

2021

0 cited

The first family with adult osteogenesis imperfecta caused by a novel homozygous mutation in CREB3L1

Q4

MOLECULAR GENETICS AND GENOMIC MEDICINE , vol. 7

Creator: Cayami F.K.

2019

5 cited

Clinical evaluation and mutation analysis in Indonesian autosomal dominant polycystic kidney disease

Q4

PAKISTAN JOURNAL OF MEDICAL AND HEALTH SCIENCES (ISSN: 19967195) , vol. 13 , pp. 908-913

Creator: Partiningrum D.

2019

0 cited

4H Leukodystrophy: Lessons from 3T Imaging

Q2

NEUROPEDIATRICS (ISSN: 0174304X) , vol. 49 , pp. 112-117

Creator: Cayami F.K.

2018

8 cited

4H Leukodystrophy: A Brain Magnetic Resonance Imaging Scoring System

Q2

NEUROPEDIATRICS (ISSN: 0174304X) , vol. 48 , pp. 152-160

Creator: Vrij-Van Den Bos S.

2017

13 cited

Optimization of pcr condition: The first study of high resolution melting technique for screening of apoa1 variance

Q2

YONAGO ACTA MEDICA (ISSN: 05135710) , vol. 60 , pp. 24-30

Creator: Wahyuningsih H.

2017

4 cited

X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1

Q2

NEUROGENETICS (ISSN: 13646745) , vol. 18 , pp. 185-194

Creator: Miyake N.

2017

28 cited