Elias, Ellen Roy
412  Ergebnisse:
Personensuche X
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1

Chronic constipation and nausea in a child:

, In: The Symptom-Based Handbook for Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders,
 
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2

Failure to thrive in a young child:

, In: The Symptom-Based Handbook for Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders,
Liu, Edwin ; Elias, Ellen Roy - p. 403-408 , 2024
 
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3

Abdominal pain and feeding intolerance in a child:

, In: The Symptom-Based Handbook for Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders,
Atkins, Dan ; Elias, Ellen Roy - p. 389-394 , 2024
 
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4

Contributors:

, In: The Symptom-Based Handbook for Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders,
Agnew, Patrick S. ; Allison, Molly S. ; Atkins, Dan... - p. xv-xxii , 2024
 
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5

23.2 Diagnosing Ehlers-Danlos Syndrome (EDS):

Elias, Ellen Roy
Journal of the American Academy of Child & Adolescent Psychiatry.  62 (2023)  10 - p. S35 , 2023
 
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7

Down syndrome:

, In: Berman's Pediatric Decision Making,
 
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8

Contributors:

, In: Berman's Pediatric Decision Making,
Abzug, Mark J. ; Albano, Edythe ; Amin, Nimisha... - p. vii-xiv , 2011
 
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9

INTELLECTUAL DISABILITY:

, In: Developmental-Behavioral Pediatrics,
Elias, Ellen Roy ; Crocker, Allen C. - p. 663-673 , 2009
 
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10

GENETIC SYNDROMES AND DYSMORPHOLOGY:

, In: Developmental-Behavioral Pediatrics,
Proud, Virginia Kent ; Elias, Ellen Roy - p. 246-257 , 2009
 
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11

BIOMEDICAL BASIS OF DEVELOPMENT AND BEHAVIOR:

, In: Developmental-Behavioral Pediatrics,
Elias, Ellen Roy - p. 209-212 , 2009
 
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12

044: Smith-Lemli-Opitz syndrome—retinal pigment epithelial ..:

Braverman, Rebecca ; Curtis, Theodore ; Drack, Arlene...
Journal of American Association for Pediatric Ophthalmology and Strabismus.  13 (2009)  1 - p. e12 , 2009
 
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13

CHILDREN WITH MULTIPLE DISABILITIES AND SPECIAL HEALTH CARE..:

, In: Developmental-Behavioral Pediatrics,
Elias, Ellen Roy - p. 737-745 , 2009
 
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15

Response to ?Cholesterol supplementation in Smith-Lemli-Opi..:

Elias, Ellen Roy
American Journal of Medical Genetics.  78 (1998)  4 - p. 379-380 , 1998
 
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