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Results of search for 'au:"Demirkol, M"', page 1 of 2
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Authors
Adalet, I
Baykal, T
Böhles, H
Cantez, S
Coskun, T
Coşkun, T
Demir, F
Demirkol, M
Demirkol, M O
Dursun, A
Giovannini, M
Gokcay, G
Gokdemir, Y
Hüner, G
Jensen, K
Kalkanoğlu, H S
Ozalp, I
Sewell, A C
Tokatli, A
Wolf, B
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Topics
Adolescent
Adult
Amidohydrolases
Amino Acid Metabolism, Inborn Errors
Biotinidase
Child
Child, Preschool
Female
Follow-Up Studies
Genotype
Humans
Infant
Infant, Newborn
Male
Mutation
Turkey
blood
deficiency
genetics
metabolism
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English
Your search returned 32 results.
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1.
Breast milk taurine and its possible influence on the development of breast milk induced jaundice of the neonate--a hypothesis.
[electronic resource]
by
Demirkol, M
Bohles, H
Producer:
19950411
In:
Advances in experimental medicine and biology
vol. 359
Online resources:
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2.
Ocular and periorbital anthropometry in the newborn.
[electronic resource]
by
Demirkol, M
Ertuğrul, T
Neyzi, O
Producer:
19880712
In:
Human biology
vol. 60
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3.
The influence of a severe burn injury on the distribution of carnitine between blood cells.
[electronic resource]
by
Böhles, H
Demirkol, M
Sewell, A C
Producer:
19960710
In:
Burns : journal of the International Society for Burn Injuries
vol. 22
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4.
The variation of carnitine content in human blood cells during disease--a study in bacterial infection and inflammatory bowel disease.
[electronic resource]
by
Demirkol, M
Sewell, A C
Böhles, H
Producer:
19941206
In:
European journal of pediatrics
vol. 153
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5.
Breastfeeding experience in inborn errors of metabolism other than phenylketonuria.
[electronic resource]
by
Huner, G
Baykal, T
Demir, F
Demirkol, M
Producer:
20050915
In:
Journal of inherited metabolic disease
vol. 28
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6.
Incidence of biotinidase deficiency in Turkish newborns.
[electronic resource]
by
Baykal, T
Hüner, G
Sarbat, G
Demirkol, M
Producer:
19990114
In:
Acta paediatrica (Oslo, Norway : 1992)
vol. 87
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7.
Breast feeding in organic acidaemias.
[electronic resource]
by
Gokcay, G
Baykal, T
Gokdemir, Y
Demirkol, M
Producer:
20070109
In:
Journal of inherited metabolic disease
vol. 29
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8.
Follow up of phenylketonuria patients.
[electronic resource]
by
Demirkol, M
Giżewska, M
Giovannini, M
Walter, J
Producer:
20120320
In:
Molecular genetics and metabolism
vol. 104 Suppl
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9.
Intense skeletal lesions in a patient with primary hyperparathyroid disease.
[electronic resource]
by
Demirkol, M O
Birinci, H S
Kadioğlu, A
Producer:
20011011
In:
Clinical nuclear medicine
vol. 26
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10.
Neurological deterioration in patients with urea cycle disorders under valproate therapy--a cause for concern.
[electronic resource]
by
Sewell, A C
Böhles, H J
Herwig, J
Demirkol, M
Producer:
19951109
In:
European journal of pediatrics
vol. 154
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11.
Hyperchylomicronaemia due to lipoprotein lipase deficiency as a cause of false-positive newborn screening for biotinidase deficiency.
[electronic resource]
by
Santer, R
Gokçay, G
Demirkol, M
Gal, A
Lukacs, Z
Producer:
20050804
In:
Journal of inherited metabolic disease
vol. 28
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12.
Hydatid cyst of the interventricular septum: an unusual cause of a fixed myocardial perfusion defect.
[electronic resource]
by
Demirkol, M O
Kurtoğlu, N
Keleş, C
Sişmanoğlu, M
Turan, F
Producer:
20011011
In:
Clinical nuclear medicine
vol. 26
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13.
Diagnosis of brain infarction on lung perfusion scintigraphy.
[electronic resource]
by
Onur Demirkol, M
Mutlu, B
Say, B
Başaran, Y
Turan, F
Producer:
20011004
In:
Clinical nuclear medicine
vol. 26
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14.
Blood flow of free gingival grafts measured by xenon-133 clearance.
[electronic resource]
by
Demirkol, A
Demirkol, M O
Demirel, K
Meriç, H
Cantez, S
Producer:
20011205
In:
Periodontal clinical investigations : official publication of the Northeastern Society of Periodontists
vol. 23
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15.
99Tcm-tetrofosmin scintigraphy in the evaluation of palpable breast masses.
[electronic resource]
by
Adalet, I
Demirkol, M O
Müslümanoğlu, M
Bozfakioğlu, Y
Cantez, S
Producer:
19970610
In:
Nuclear medicine communications
vol. 18
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16.
Hyperhydroxyprolinaemia detected in newborn screening with tandem mass spectrometry.
[electronic resource]
by
Baykal, T
Karaaslan, I
Gokcay, G
Demir, F
Laleli, Y
Demirkol, M
Producer:
20050505
In:
Journal of inherited metabolic disease
vol. 27
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17.
Development of Kasabach-Merritt syndrome following needle aspiration of a hemangioma.
[electronic resource]
by
Karaböcüoğlu, M
Başarer, N
Aydoğan, U
Demirkol, M
Kurdoğlu, G
Neyzi, O
Producer:
19920925
In:
Pediatric emergency care
vol. 8
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18.
99Tc(m)-polyclonal IgG scintigraphy in the detection of infected hip and knee prostheses.
[electronic resource]
by
Demirkol, M O
Adalet, I
Unal, S N
Tözün, R
Cantez, S
Producer:
19970930
In:
Nuclear medicine communications
vol. 18
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19.
Effects of low-level laser therapy on osteoblastic bone formation and relapse in an experimental rapid maxillary expansion model.
[electronic resource]
by
Aras, M H
Erkilic, S
Demir, T
Demirkol, M
Kaplan, D S
Yolcu, U
Producer:
20180119
In:
Nigerian journal of clinical practice
vol. 18
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20.
Molecular aspects of glycogen storage disease type Ia in Turkish patients: a novel mutation in the glucose-6-phosphatase gene.
[electronic resource]
by
Hüner, G
Podskarbi, T
Schütz, M
Baykal, T
Sarbat, G
Shin, Y S
Demirkol, M
Producer:
19981130
In:
Journal of inherited metabolic disease
vol. 21
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