Search Results - "Chahin, S."
-
1
Central vein sign: A diagnostic biomarker in multiple sclerosis (CAVS-MS) study protocol for a prospective multicenter trial
Published in NeuroImage clinical (01-01-2021)“…•Approximately one in five patients with MS do not have the disease.•The central vein differentiates multiple sclerosis from other white matter lesions.•The…”
Get full text
Journal Article -
2
Specialty tier cost sharing and use of disease modifying Therapies Among Medicare Beneficiaries with Multiple Sclerosis
Published in Value in health (01-05-2015)Get full text
Journal Article -
3
Acute disseminated encephalomyelitis in China, Singapore and Japan: a comparison with the USA
Published in European journal of neurology (01-02-2017)“…Background and purpose Ethnicity‐related differences in the incidence of acute disseminated encephalomyelitis (ADEM) and other demyelinating diseases including…”
Get full text
Journal Article -
4
-
5
PDB13 Short Stature in Turner Syndrome: Basal Characteristics and Follow-Up of a Colombian Cohort
Published in Value in health (01-06-2012)Get full text
Journal Article -
6
Integrated Behavioral Health Care: Reflections of the Past
Published in The Pediatric clinics of North America (01-06-2021)Get full text
Journal Article -
7
-
8
Autism spectrum disorder: psychological and functional assessment, and behavioral treatment approaches
Published in Translational pediatrics (01-02-2020)“…There have been significant changes in the way Autism has been defined especially in the last decade. The changes encompass criteria over a spectrum rather…”
Get full text
Journal Article -
9
Palatal Myoclonus Secondary to Vertebral Artery Compression of the Inferior Olive
Published in Journal of neuroimaging (01-10-2000)“…A 47‐year‐old male with a 5‐year history of palatal myoclonus was found on magnetic resonance imaging (MRI) exa mination to have an ectatic dominant left…”
Get full text
Journal Article -
10
Elevation of serum luteinizing hormone levels during hydrocortisone treatment in infant girls with 21-hydroxylase deficiency
Published in Acta pædiatrica (Oslo) (01-10-1996)“…During the first months of postnatal life serum luteinizing hormone (LH) levels in girls are lower than in boys. The mechanism of this sex difference is not…”
Get more information
Journal Article -
11
PND67 - Specialty tier cost sharing and use of disease modifying Therapies Among Medicare Beneficiaries with Multiple Sclerosis
Published in Value in health (01-05-2015)Get full text
Journal Article -
12
-
13
Colombian reference growth curves for height, weight, body mass index and head circumference
Published in Acta Paediatrica (01-03-2016)“…Aim Published Growth studies from Latin America are limited to growth references from Argentina and Venezuela. The aim of this study was to construct reference…”
Get full text
Journal Article -
14
Serum concentrations of follicle stimulating hormone and luteinizing hormone in normal girls and boys during prepuberty and at early puberty
Published in Journal of endocrinological investigation (01-02-1996)“…Serum luteinizing hormone (LH) and follicle stimulating hormone (FSH) morning levels were determined in 327 normal prepubertal and early pubertal children of…”
Get full text
Journal Article -
15
Visual Evoked Potential Latency Prolongation in MS: Correlation with Cognitive Performance on a Computerized Testing Battery (P07.260)
Published in Neurology (26-04-2012)“…Abstract only…”
Get full text
Journal Article -
16
Integrated Behavioral Health Care
Published in The Pediatric clinics of North America (01-06-2021)Get full text
Journal Article -
17
-
18
An Examination of Medical Resident Practices Regarding Patient Communication About Infant Safe Sleep Practices
Published 01-01-2022“…Infant mortality is a significant public health concern in the United States, particularly because of the large racial disparities in death rates. In…”
Get full text
Dissertation -
19
12 SERUM LH AND FSH DURING THE FIRST TRIMESTER OF LIFE IN NORMAL (C) CHILDREN AND IN AMBIGUOUS GENITALIA
Published in Pediatric research (01-11-1994)Get full text
Journal Article -
20
Caracterización de las mutaciones del gen de la 21-hidroxilasa en familias colombianas
Published in Acta biológica colombiana (01-07-2001)“…La deficiencia de la 21-Hidroxilasa 21(OH) es la causa más frecuente de Hiperplasia SuprarenalCongénita. Aproximadamente 75% de los casos son causados por…”
Get full text
Journal Article