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Publications by Imane Cherkaoui Jaouad
Hyaline Fibromatosis Syndrome With Mutation C.1074delT of the CMG2 Gene: A Case Report
Journal of Medical Case Reports
Medicine
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Juvenile Hyaline Fibromatosis Management With a Diode Laser: A Rare Case Report
Journal of Lasers in Medical Sciences
Sports Medicine
Nephrology
Orthopedics
Dentistry
Dermatology
Urology
Surgery
Juvenile Hyaline Fibromatosis
Juvenile Hyaline Fibromatosis
Apert Syndrome With FGFR2 758 C > G Mutation: A Chinese Case Report
Frontiers in Genetics
Genetics
Molecular Medicine
BCS1L Gene Mutation Causing GRACILE Syndrome: Case Report
Renal Failure
Medicine
Nephrology
Critical Care
Intensive Care Medicine
A New Mutation in IDS Gene Causing Hunter Syndrome: A Case Report
Frontiers in Genetics
Genetics
Molecular Medicine
A Rare C.183_187dupCTCAC Mutation of the Acetylcholine Receptor CHRNE Gene in a South Asian Female With Congenital Myasthenic Syndrome: A Case Report
BMC Neurology
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Homozygous R396H Mutation of the RAG1 Gene in a Saudi Infant With Omenn's Syndrome: A Case Report
Cases Journal
Neurodevelopmental Stimulation of a Child With a Noonan Syndrome With a Non-Frequent Mutation in RAF1 Gene — Case Report
The Journal of Neurological and Neurosurgical Nursing