Suchergebnisse - "Kornitzer, Jeffrey"

PubPharm (19)

1

Moya moya vasculopathy and MECP2 duplication syndrome

enthalten in: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery | 2024

von Holover, G. | Adams, D. | Milligan, D. | +4

2

COVID-19 in Pediatric Inpatients : A Multi-Center Observational Study of Factors Associated with Negative Short-Term Outcomes

enthalten in: Children (Basel, Switzerland) | 2021

von Rubenstein, S. | Grew, E. | Clouser, K. | +5

3

A Systematic Review of Characteristics Associated with COVID-19 in Children with Typical Presentation and with Multisystem Inflammatory Syndrome

enthalten in: International journal of environmental research and public health | 2021

von Kornitzer, J. | Johnson, J. | Yang, M. | +4

4

Differentiating Flail Limb Syndrome From Amyotrophic Lateral Sclerosis

enthalten in: American journal of physical medicine & rehabilitation | 2020

von Kornitzer, J. | Abdulrazeq, H. | Zaidi, M. | +5

5

The Quality of YouTube Videos as an Educational Resource for Attention-Deficit/Hyperactivity Disorder

enthalten in: Pediatric neurology | 2020

von Ward, M. | Ward, B. | Warren, C. | +4

6

Clinical Presentation and Outcome in Autoimmune Encephalitis Associated With N-Type Voltage-Gated Calcium Channels in Children

enthalten in: Journal of child neurology | 2019

von Kornitzer, J. | Taha, F. | Segal, E.

7

Distal 1q21.1 and proximal 1q21.2 microduplication in a child with attention-deficit hyperactivity disorder

enthalten in: Acta neurologica Belgica | 2019

von Veerapandiyan, A. | Oh, D. | Kornitzer, J.

8

A novel intronic homozygous mutation in the AMT gene of a patient with nonketotic hyperglycinemia and hyperammonemia

enthalten in: Metabolic brain disease | 2019

von Silverstein, S. | Veerapandiyan, A. | Hayes-Rosen, C. | +2

9

A novel intronic homozygous mutation in the AMT gene of a patient with nonketotic hyperglycinemia and hyperammonemia

enthalten in: Metabolic brain disease | 2018

von Silverstein, S. | Veerapandiyan, A. | Hayes-Rosen, C. | +2

10

A novel intronic homozygous mutation in the AMT gene of a patient with nonketotic hyperglycinemia and hyperammonemia

enthalten in: Metabolic brain disease | 2018

von Silverstein, S. | Veerapandiyan, A. | Hayes-Rosen, C. | +2