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Nederlands Tijdschrift Voor Geneeskunde
|
October 29, 1988
[2 patients with Reye syndrome?]
R H Houwen, G F Nelck, D J Reijngoud, et al.
Journal of the Neurological Sciences
|
June 1, 1994
Extreme variability of clinical symptoms among sibs in a MELAS family correlated with heteroplasmy for the mitochondrial A3243G mutation
D de Vries, I de Wijs, W Ruitenbeek, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1998
Neutropenia and neutrophil dysfunction in glycogen storage disease type 1c
G Visser, J Herwig, J P Rake, et al.
Ocular Immunology and Inflammation
|
November 20, 2019
The Role of <sup>18</sup>F-FDG PET/CT in Suspected Intraocular Sarcoidosis and Tuberculosis
C Burger, J L Holness, D P Smit, et al.
Frontiers in Ophthalmology
|
July 10, 2024
CXCL13, CXCL10 and CXCL8 as Indicators of Ocular and Neurological Involvement in Patients With Ocular Syphilis: An Observational Descriptive Study
Laurie W van der Merwe, Candice Snyders, Martin Kidd, et al.
Acta Crystallographica. Section E, Crystallographic Communications
|
May 8, 2026
Nirmatrelvir methyl <i>tert</i>-butyl ether solvate
Jared P Smit, Dale K Purcell, David A Engers, et al.
Ocular Immunology and Inflammation
|
April 24, 2024
Vogt-Koyanagi-Harada Disease
Ilknur Tugal-Tutkun, Derrick P Smit, Ahmed M Abu El-Asrar, et al.
Pediatric Research
|
June 15, 1999
A convenient diagnostic function test of peripheral blood neutrophils in glycogen storage disease type Ib
A J Verhoeven, G Visser, R van Zwieten, et al.
European Journal of Pediatrics
|
December 1, 1988
Mevalonate kinase deficiency in a child with cerebellar ataxia, hypotonia and mevalonic aciduria
K M Gibson, G Hoffmann, W L Nyhan, et al.
Tijdschrift Voor Kindergeneeskunde
|
October 1, 1993
[Late diagnosis of classical galactosemia. An adult with special biochemistry]
J J Weits-Binnerts, R Hordijk, G P Smit, et al.
Page
of 26
Search research articles
Search
Showing results (151-160 of 255) with videos related to
Sort By:
Page
of 26
Nederlands Tijdschrift Voor Geneeskunde
|
October 29, 1988
[2 patients with Reye syndrome?]
R H Houwen, G F Nelck, D J Reijngoud, et al.
Journal of the Neurological Sciences
|
June 1, 1994
Extreme variability of clinical symptoms among sibs in a MELAS family correlated with heteroplasmy for the mitochondrial A3243G mutation
D de Vries, I de Wijs, W Ruitenbeek, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1998
Neutropenia and neutrophil dysfunction in glycogen storage disease type 1c
G Visser, J Herwig, J P Rake, et al.
Ocular Immunology and Inflammation
|
November 20, 2019
The Role of <sup>18</sup>F-FDG PET/CT in Suspected Intraocular Sarcoidosis and Tuberculosis
C Burger, J L Holness, D P Smit, et al.
Frontiers in Ophthalmology
|
July 10, 2024
CXCL13, CXCL10 and CXCL8 as Indicators of Ocular and Neurological Involvement in Patients With Ocular Syphilis: An Observational Descriptive Study
Laurie W van der Merwe, Candice Snyders, Martin Kidd, et al.
Acta Crystallographica. Section E, Crystallographic Communications
|
May 8, 2026
Nirmatrelvir methyl <i>tert</i>-butyl ether solvate
Jared P Smit, Dale K Purcell, David A Engers, et al.
Ocular Immunology and Inflammation
|
April 24, 2024
Vogt-Koyanagi-Harada Disease
Ilknur Tugal-Tutkun, Derrick P Smit, Ahmed M Abu El-Asrar, et al.
Pediatric Research
|
June 15, 1999
A convenient diagnostic function test of peripheral blood neutrophils in glycogen storage disease type Ib
A J Verhoeven, G Visser, R van Zwieten, et al.
European Journal of Pediatrics
|
December 1, 1988
Mevalonate kinase deficiency in a child with cerebellar ataxia, hypotonia and mevalonic aciduria
K M Gibson, G Hoffmann, W L Nyhan, et al.
Tijdschrift Voor Kindergeneeskunde
|
October 1, 1993
[Late diagnosis of classical galactosemia. An adult with special biochemistry]
J J Weits-Binnerts, R Hordijk, G P Smit, et al.
Page
of 26