12th congress of pediatric inherited metabolic disorders and endocrinology, آبان ماه ۱۳۹۸

12th congress of pediatric inherited metabolic disorders and endocrinology

12th congress of pediatric inherited metabolic disorders and endocrinology

12th congress of pediatric inherited metabolic disorders and endocrinology In date 2019-11-06 by ,مركز تحقيقات رشد و تكامل كودكان in City Tehran was held. please refer to the following link to download all the papers of conference proceedings: _PROCEEDINGS 12th congress of pediatric inherited metabolic disorders and endocrinology

Accepted papers in 12th congress of pediatric inherited metabolic disorders and endocrinology

• Newly in diagnosis of type 1 diabetes mellitus

• Clinical, Laboratory Data & Outcome Of 7 Patients Affected Of Multiple Acyl-Coa Dehydrogenase Dehydrogenase

• Clinical, Laboratory, Molecular Data and Miglustat Outcome in 8 Iranian patients affected of Niemann Pick Type C

• Dyslipidemia and microbiota

• Efficacy of BCG vaccine for treatment of type1 diabetes

• A New Case of 3 –Hydroxyisobutyryl-CoA Hydrolase (HIBCH) Deficiency

• Niemann-Pick disease Type C

• A new treatment for 2-ketoglutaric aciduria: a case report

• Self-Care Education Effect on Patient Quality of Life with Phenyl Ketone Urea in Medical Center in Tehran, Iran

• Seizure pattern in Inborn Error of Metabolic Disorders

• How to diagnose and treat Tyrosinemia type 1

• Frequency of diabetic ketoacidosis in new cases of type 1 diabetes in children hospitalized in Pediatric Hospital from 2006 to 2019

• Transient and permanent hypothyroidism in Iran: what are the associated factors

• Early and Delayed puberty among Iranian children with obesity

• Organic Acidemia

• Metabolic Disorders, Genetic Abnormalities and Ophthalmology

• The Effects of Urtica Dioica on Diabetes

• Epidermal Nevus Syndrome AND Hypophosphatemic rickets

• New treatment strategies for lysosomal storage disorders

• Gaucher disease

• Diagnosis of a rare ciliopathy by genetic test -WHOLE EXOME SEQUENCING- in a nonconsanguineous marriage family: case report

• Obstructive Gastrointestinal Tract Disorders in cystic fibrosis

• Diagnosis of Primary Ciliary Dyskinesia by the identification of homozygote mutation in CCDC40 gene with whole-exome sequencing in a 12 years old patient: a case report

• How can we interpret metabolic tests

• غدد، معرفی یک مورد اختلال رشد و هیپوگلیسمی

• مقایسه دیابت بارداری وابسته به مصرف انسولین با دیابت بارداری وابسته به مصرف متفورمین و اثر آنها بر مارکرهای غربالگری سه ماهه اول بارداری در سال های 1387 تا 1398 در تهران

• دارو درمانی بیماران منتخب متابولیک؛ آیا درست انجام می دهیم

• غربالگری بیماری های متابولیک ارثی نوزادان

• Challenges of Family of Children with Phenylketonuria and its Impact on their Mental Health

• Clinical evaluation of the effect of restorative topical ointment on the process of open cutaneous wound healing on diabetic children: A double-blind randomized clinical triae

• خود مراقبتی در کودکان مبتلا به دیابت نوع 1

• چالش های پیش روی والدین کودکان مبتلا به اختلالات متابولیک

• بررسی ویژگی های روان سنجی ابزار اندازه گیری مدیریت خانواده ( FaMM ) و کاربرد آن در بررسی مدیریت خانواده در بیماری های مزمن دوره کودکی: مقاله مروری

• تعییین رضایتمندی والدین کودکان بستری در بخش غدد از مراقبت های پرستاری ارائه شده

• مروری بر عملکرد پرستاران در ارائه مراقبت های تسکینی در کودکان مبتلا به دیابت نوع 1

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