Damayanti Rusli Sjarif: Perbedaan antara revisi

Konten dihapus Konten ditambahkan
Nein (bicara | kontrib)
k →‎Hasil karya: lengkap (semoga)
Nein (bicara | kontrib)
k →‎Hasil karya: kecilkan nama jurnal dan tebalkan volume
Baris 6:
==Hasil karya==
 
* Damayanti R Sjarif, Christina Hellerud, Johannes K Ploos van Amstel, Willem J Kleijer, Wolfgang Sperl, Didier Lacombe, Jõrn Oliver Sass, Frits A Beemer, Marinus Duran and Bwee Tien Poll-The, ''Glycerol kinase deficiency: residual activity explained by reduced transcription and enzyme conformation'', [http://www.nature.com/ejhg/journal/v12/n6/full/5201172a.html European Journal of Human Genetics, June 2004, Volume '''12''', Number 6, Pages 424-432]
 
* D. R. Sjarif, L. Dorland, W. Sperl, T. J. de Koning, F. A. Beemer, B. T. Poll-The und M. Duran, ''Hyperketonaemia in glycerol kinase deficiency'', Journal of Inherited Metabolic Disease, Volume '''23''', Number 7 / November 2000, DOI [http://dx.doi.org/10.1023/A:1005680211483 10.1023/A:1005680211483]
 
* Sjarif DR, ''Inborn errors of metabolism in Indonesia'', Journal of Inherited Metabolic Disease '''29''': 25-25 Suppl. 1 AUG 2006
 
* Prawitasari T, Sjarif DR, ''Clinical improvement after administration of carnitine and ubiquinone in possible respiratory chain disorders'', JOURNALJournal OFof INHERITEDInherited METABOLICMetabolic DISEASEDisease '''29''': 116-116 Suppl. 1 AUG 2006
 
* Sudewi NP, Sjarif DR, ''Metabolic acidosis and failure to thrive'', Journal of Inherited Metabolic Disease '''29''': 121-121 Suppl. 1 AUG 2006
JOURNAL OF INHERITED METABOLIC DISEASE 29: 121-121 Suppl. 1 AUG 2006
 
* Indawati W, Sjarif DR, ''Intelligence impairment in Morquio syndrome type IVA: A case report'', JOURNALJournal OFof INHERITEDInherited METABOLICMetabolic DISEASEDisease '''29''': 149-149 Suppl. 1 AUG 2006
 
* Sjarif DR, Hutapea E, ''A Bataknese family of two siblings with Sanfilippo syndrome: First case report in Ciptomangunkusumo Hospital, Jakarta, Indonesia '', JOURNALJournal OFof INHERITEDInherited METABOLICMetabolic DISEASEDisease '''29''': 149-149 Suppl. 1 AUG 2006
 
* Meilany TA, Prawitasari T, Sjarif DR, ''A child with suspected Morquio syndrome: A challenge to established diagnosis'', JOURNALJournal OFof INHERITEDInherited METABOLICMetabolic DISEASEDisease '''29''': 152-152 Suppl. 1 AUG 2006
 
* Sjarif DR, Revesz T, de Koning TJ, et al. ''Isolated glycerol kinase deficiency and Fanconi anemia'', AMERICANAmerican JOURNALJournal OFof MEDICALMedical GENETICSGenetics '''99''' (2): 159-160 MAR 1 2001
 
* Sjarif DR, Dorland L, Sperl W, et al., ''Hyperketonaemia in glycerol kinase deficiency'', JOURNALJournal OFof INHERITEDInherited METABOLICMetabolic DISEASEDisease '''23''' (7): 760-764 NOV 2000
 
* Sjarif DR, van Amstel JKP, Duran M, et al., ''Isolated and contiguous glycerol kinase gene disorders: A review'', JOURNALJournal OFof INHERITEDInherited METABOLICMetabolic DISEASEDisease '''23''' (6): 529-547 SEP 2000
 
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