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Timothy E Lotze

Showing results (11-20 of 59) with videos related to

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Journal of Child Neurology|August 24, 2012
Pediatric acute transverse myelitis overview and differential diagnosisVarina L Wolf, Pamela J Lupo, Timothy E Lotze
American Journal of Medical Genetics. Part A|April 11, 2012
A child with an inherited 0.31 Mb microdeletion of chromosome 14q32.33: further delineation of a critical region for the 14q32 deletion syndromeJ Lloyd Holder, Timothy E Lotze, Carlos Bacino, et al.
Pediatric Radiology|September 1, 2018
Ultrasound-guided cervical puncture for nusinersen administration in adolescentsCarlos B Ortiz, Kamlesh U Kukreja, Timothy E Lotze, et al.
Journal of Pediatric Orthopedics. Part B|March 20, 2012
Hyperkalemic cardiac arrest in a 14-month-old following spica cast applicationMohan V Belthur, Carlos J Campos, Timothy E Lotze, et al.
Journal of Pediatric Psychology|October 20, 2017
Health-Related Quality of Life in Pediatric Patients With Demyelinating Diseases: Relevance of Disability, Relapsing Presentation, and FatigueMariella M Self, Aaron Fobian, Katherine Cutitta, et al.
Journal of Child Neurology|April 11, 2019
Global Health Education in Child Neurology and Neurodevelopmental Disabilities Training Programs in the United States: A National SurveyAndres Jimenez-Gomez, Robert C Stowe, Alfred Balasa, et al.
Journal of Child Neurology|July 4, 2017
The Experience of Families With Children With Spinal Muscular Atrophy Type I Across Health Care SystemsDiane V Murrell, Timothy E Lotze, Harold J Farber, et al.
Journal of Pediatric Nursing|September 30, 2018
Identifying Opportunities to Provide Family-centered Care for Families With Children With Type 1 Spinal Muscular AtrophyDiane V Murrell, Claire A Crawford, Chanti T Jackson, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|February 25, 2021
Double Vision and Gait Ataxia in an Immunocompetent 9-Year-Old Girl With Intracranial PhaeohyphomycosisAishwarya V Pareek, Timothy E Lotze, Gail Demmler, et al.
Archives of Neurology|February 16, 2005
Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiencySeema R Lalani, Georgirene D Vladutiu, Katie Plunkett, et al.
Pageof 6

Showing results (11-20 of 59) with videos related to

Sort By:
Pageof 6
Journal of Child Neurology|August 24, 2012
Pediatric acute transverse myelitis overview and differential diagnosisVarina L Wolf, Pamela J Lupo, Timothy E Lotze
American Journal of Medical Genetics. Part A|April 11, 2012
A child with an inherited 0.31 Mb microdeletion of chromosome 14q32.33: further delineation of a critical region for the 14q32 deletion syndromeJ Lloyd Holder, Timothy E Lotze, Carlos Bacino, et al.
Pediatric Radiology|September 1, 2018
Ultrasound-guided cervical puncture for nusinersen administration in adolescentsCarlos B Ortiz, Kamlesh U Kukreja, Timothy E Lotze, et al.
Journal of Pediatric Orthopedics. Part B|March 20, 2012
Hyperkalemic cardiac arrest in a 14-month-old following spica cast applicationMohan V Belthur, Carlos J Campos, Timothy E Lotze, et al.
Journal of Pediatric Psychology|October 20, 2017
Health-Related Quality of Life in Pediatric Patients With Demyelinating Diseases: Relevance of Disability, Relapsing Presentation, and FatigueMariella M Self, Aaron Fobian, Katherine Cutitta, et al.
Journal of Child Neurology|April 11, 2019
Global Health Education in Child Neurology and Neurodevelopmental Disabilities Training Programs in the United States: A National SurveyAndres Jimenez-Gomez, Robert C Stowe, Alfred Balasa, et al.
Journal of Child Neurology|July 4, 2017
The Experience of Families With Children With Spinal Muscular Atrophy Type I Across Health Care SystemsDiane V Murrell, Timothy E Lotze, Harold J Farber, et al.
Journal of Pediatric Nursing|September 30, 2018
Identifying Opportunities to Provide Family-centered Care for Families With Children With Type 1 Spinal Muscular AtrophyDiane V Murrell, Claire A Crawford, Chanti T Jackson, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|February 25, 2021
Double Vision and Gait Ataxia in an Immunocompetent 9-Year-Old Girl With Intracranial PhaeohyphomycosisAishwarya V Pareek, Timothy E Lotze, Gail Demmler, et al.
Archives of Neurology|February 16, 2005
Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiencySeema R Lalani, Georgirene D Vladutiu, Katie Plunkett, et al.
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