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Journal of Inherited Metabolic Disease
|
July 18, 2002
Maple syrup urine disease: mutation analysis in Turkish patients
A Dursun, M Henneke, K Ozgül, et al.
Human Genetics
|
January 12, 2001
Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE)
A Romstad, H S Kalkanoğlu, T Coşkun, et al.
JIMD Reports
|
February 23, 2013
Identification of mutations and evaluation of cardiomyopathy in Turkish patients with primary carnitine deficiency
M Kilic, R K Ozgül, T Coşkun, et al.
International Journal of Pediatric Otorhinolaryngology
|
December 13, 2006
Audiologic findings in children with biotinidase deficiency in Turkey
G A Genc, H S Sivri-Kalkanoğlu, A Dursun, et al.
Journal of Microencapsulation
|
November 1, 1994
Effect of encapsulation of chloramphenicol in albumin microspheres on its in vitro transfer across the human placenta
M A Onur, I Vural, N Başçi, et al.
JIMD Reports
|
February 23, 2013
Mutation spectrum of fumarylacetoacetase gene and clinical aspects of tyrosinemia type I disease
A Dursun, R K Ozgül, S Sivri, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
August 29, 2000
Endothelin-1-induced PMN infiltration and mucosal dysfunction in the rat small intestine
B K Oktar, T Coşkun, A Bozkurt, et al.
Orphanet Journal of Rare Diseases
|
July 2, 2020
PKU dietary handbook to accompany PKU guidelines
A MacDonald, A M J van Wegberg, K Ahring, et al.
Orphanet Journal of Rare Diseases
|
September 3, 2020
Correction to: PKU dietary handbook to accompany PKU guidelines
A MacDonald, A M J van Wegberg, K Ahring, et al.
Molecular Genetics and Metabolism
|
May 16, 2025
European guidelines on diagnosis and treatment of phenylketonuria: First revision
A M J van Wegberg, A MacDonald, K Ahring, et al.
Page
of 8
Search research articles
Search
Showing results (71-80 of 80) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 80 results.
Journal of Inherited Metabolic Disease
|
July 18, 2002
Maple syrup urine disease: mutation analysis in Turkish patients
A Dursun, M Henneke, K Ozgül, et al.
Human Genetics
|
January 12, 2001
Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE)
A Romstad, H S Kalkanoğlu, T Coşkun, et al.
JIMD Reports
|
February 23, 2013
Identification of mutations and evaluation of cardiomyopathy in Turkish patients with primary carnitine deficiency
M Kilic, R K Ozgül, T Coşkun, et al.
International Journal of Pediatric Otorhinolaryngology
|
December 13, 2006
Audiologic findings in children with biotinidase deficiency in Turkey
G A Genc, H S Sivri-Kalkanoğlu, A Dursun, et al.
Journal of Microencapsulation
|
November 1, 1994
Effect of encapsulation of chloramphenicol in albumin microspheres on its in vitro transfer across the human placenta
M A Onur, I Vural, N Başçi, et al.
JIMD Reports
|
February 23, 2013
Mutation spectrum of fumarylacetoacetase gene and clinical aspects of tyrosinemia type I disease
A Dursun, R K Ozgül, S Sivri, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
August 29, 2000
Endothelin-1-induced PMN infiltration and mucosal dysfunction in the rat small intestine
B K Oktar, T Coşkun, A Bozkurt, et al.
Orphanet Journal of Rare Diseases
|
July 2, 2020
PKU dietary handbook to accompany PKU guidelines
A MacDonald, A M J van Wegberg, K Ahring, et al.
Orphanet Journal of Rare Diseases
|
September 3, 2020
Correction to: PKU dietary handbook to accompany PKU guidelines
A MacDonald, A M J van Wegberg, K Ahring, et al.
Molecular Genetics and Metabolism
|
May 16, 2025
European guidelines on diagnosis and treatment of phenylketonuria: First revision
A M J van Wegberg, A MacDonald, K Ahring, et al.
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of 8