Regentime

Regentime

Beirut, Lebanon


Focus Area: Regentime | Diabetes | Heart Disease | Liver Disease | Neurological Diseases | Alzheimer's Disease | Parkinson's Disease | Arthritis | Joint Diseases | Vision Disorders | Lupus | Diabetes | Autism | Muscular Dystrophy | Cerebral Palsy | Multiple Sclerosis | Beirut, Lebanon Muscular Dystrophy, Parkinson's, Alzheimer's, ALS, Multiple Sclerosis, Autism, Chronic Diseases, Diabetes, Cerebral Palsy, Lebanon

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Regentime is a procedure developed by Nassim Abi Chahine, M.D, a renowned neurosurgeon in Lebanon. Regentime aims at helping patients with incurable diseases have a new hope for their recovery and treatment. 

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Regentime is a technique which can relieve symptoms or in some cases cure the disease itself, with minimal and sometimes no side effects. The positive results of this procedure are usually felt 2-4 months after the procedure depending on the condition treated and how severe it is.

 

 

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Some of the medical conditions treated by Regentime techniques are:

  • Arteriosclerosis
  • Autism
  • Cerebral palsy
  • Diabetes
  • Coronary artery diseases
  • Epilepsy
  • Liver cirrhosis
  • Macular Degeneration
  • Pulmonary diseases
  • Multiple Sclerosis
  • Parkinson’s disease
  • Spinal Muscular Atrophy
 
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Regentime Treatment Costs an average of 12.000 USD
 
 
 
The Regentime Procedure is continuously improved and modernized by Dr. Nassim himself. He customizes the Regentime procedure according to each patient's needs and usually it takes up to 5 days for the procedure to be completed.

 

Regentime basic cost includes: 
 
  • Case study at the highest expertise level
  • Pre-operative supervised care
  • Laboratory work and processing
  • Post-operative care

 

 

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The Regentime treatment is for many the last resort in treating or improving  chronic diseases. Dr. Nassim will answer any question you might have regarding this procedure, helping you understand how it works and what are the benefits in your case.

We are here to help you!

Click the Contact Us button and you will get all your answers and a chance to a new, healthy life!

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Details

regentim stem cell therapy clinic lebanon beirut europe middle east title

 

Regentime clinic aims at helping patients with chronic diseases such as cerebral palsy, multiple sclerosis, autism, Parkinson's, diabetes, epilepsy,  cirrhosis or macular degeneration, improve the symptoms, if not even cure the disease entirely.

Stem Cell Therapy Lebanon Beirut
 

Dr. Nassim and his experienced medical team, has helped numerous patients suffering fromchronic diseases. Improving the symptoms of a disease or even curing it has been proven to be possible thanks to Regentime therapy.

 

We are here to help you!

Click the Contact Us button and you will get all your answers and a chance to a new, healthy life!

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Treatments

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Acatalasia/ Takahara’s disease
Activator Deficiency
Acute intermittent porphyria
Acyl-CoA oxidase deficiency
Addison disease
Adrenoleukodystrophy
Adult Refsum disease
Alexander disease
Alkaptonurira
Allan-Herndon-Dudley syndrome
5-alpha-reductase deficiency
Alpha-methylcayl-CoA racemase deficiency
Alpha-mannosidosis
Aminoacylase 1 deficiency
Amyloidosis
Amyotrophic lateral sclerosis
Andersen’s disease
Anoxic brain damage
Apparent mineralocorticoid excess syndrome
Argininemia
Argininosuccinic aciduria
Arnold-Chiari malformation outcomes
Aromatase deficiency
Aromatase excess syndrome
Arteriosclerosis
Aspartylglucosaminuria
Asperger syndrome
Asthma
Ataxia
Atherosclerosis
Atopic dermatitis, eczema
Atrophic gastritis
Atrophic vaginitis
Autism
Balint’s syndrome
Batten-Spielmeyer-Sjögren-Vogt
Behçet's disease
Bernard-Soulier syndrome
Best's Disease
Beta-mannosidosis
Betaketothiolase deficiency
Biotinidase deficiency
Brunner’s syndrome
Bullous emphysema
Bullous pemphigoid
Burns (Classic thermal and frostbite)
Canavan disease
Carbamoyl-phosphate synthase I deficiency
Cardiac insufficiency
Cardiomyopathy
Carnitine-acylcarnitine translocase deficiency
Carnitine palmitoyltransferase deficiency
Carnosenemia
Cerebral amyloid angiopathy
Cerebral palsy
Cerebrotendineous xanthomatosis
Cerebrovascular diseases
Charles Bonnet Syndrome
Chemotherapy side effects (post chemotherapy)
Childhood disintegrative disorder
Cholesteryl ester storage disease
Chondroplasias- maintenance therapy
Chronic Critical Limb Ischemia
Chronic Hexosaminidase A Deficiency
Citrullinemia
Coenzyme A dehydrogenase deficiency
Color blindness
Cone-rod dystrophy
Congenital adrenal hyperplasia
congenital dyserythropoietic anemia
Congenital erythropoietic porphyria
Congenital hemolytic anemia (nonspherocytic)
Congestive heart failure
Coronary artery diseases
Cortical visual impairment
Cori’s disease
Crigler-Najjar symdrome
Crohn’s diseases
Cystathioninuria
Cystic fibrosis
Cystinosis
D-bifunctional protein deficiency
Danon disease
Dehydroxyacetonephosphate acyltransferase def
Dementia
Dermatomyositis
Diabetes Mellitus type 1
Diabetes Mellitus type 2
Diabetic Neuropathy
Dienoyl-CoA reductase deficiency
Dopamine Beta hydroxylase deficiency
Dubin-Johnson syndrome
Enthesitis, chronic
Epilepsy
Erythropoetic porphyria
Ethylmalonic encephalopathy
Fabry disease
Factor V deficiency, Owren disease
Factor X deficiency/Amyloid purpura
Familial alpha-lipoprotein deficiency
Familial male-limited precocious puberty
Fanconi-Bickel’ syndrome
Fanconi syndrome/ Oculocerebrorenal syndrome
Farber disease
Follicle-stimulating hormone insensitivity
Forbes’ disease
Fructose intolerance
Fucosidosis
Fumarase deficiency
G6PD/ Favism
Galactosemia
Galactosialidosis
Gangliosidosis (GM1)
Gaucher Disease
Glucocorticoid remedial aldosteronism
Gonadotropin-releasing hormone insensitivity
Goodpasture’s syndrome
Glanzmann's thrombasthenia
Glutaric acidemia
Glycogen storage disease
Gout, severe and recurrent cases
Hartnup disease
Hashimoto’s thyroiditis, refractory cases
Hawkinsinuria
Heart failure
Hemophilia
Hereditary CNS demyelinating disease
Hereditary coproporphyria
Hereditary Fructose intolerance
Hermansky–Pudlak syndrome
Hers’ disease
Hexosaminidase A Deficiency
Histidenemia
Homocystinuria
Huntington’s disease
Hunter syndrome
Hurler Syndrome
Hyaluronidase Deficiency
4-Hydroxy-butyric aciduria (SSADHD)
2-Hydroxy-glutaric aciduria
3-hydroxy-3-methylglutaryl-CoA lyase deficiency
Hyperargininemia
Hyperargininuria
Hyperhomocysteinuria
Hyperlysinemias
Hypermethioninemia
Hyperoxaluria/ Bird’s disease
Hyperprolinemia
Hypertrophic emphysema
Hypertryptophanemia
Hyperurecemia
Hypervalenemia
Hypo-alpha-lipoproteinemia
Iminoglycinuria
Inborn errors of steroid metabolism
Infantile Free Sialic Acid Storage Disease
Infantile Refsum disease
Intractable wound healing
Interstitial lung disease
Ionizing radiation injury
Isobutyryl-CoA dehydrogenase deficiency
Isolated 17,20-lyase deficiency
Isovaleric acIdemia
Jansky-Bielschowsky disease
Joint regeneration
Juvenile arthritis
Juvenile Hexosaminidase A Deficiency
Kernicterus- Bilirubin encephalopathy
Krabbe disease
Kufs disease
Lactose intolerance
Leber's congenital amaurosis
Lesch-Nyhan syndrome
Leukopdystrophies
Leukoencephalopathy
Leydig cell hypoplasia
Lipoid congenital adrenal hyperplasia
Liver cirrhosis
Locked-in syndrome
Lysinuric protein intolerance
Lysosomal storage disease
Lysosomal acid lipase deficiency
Macular Degeneration
Malonyl-CoA decarboxylase deficiency
Mannosidosis
Maple syrup urine disease
Maroteaux-Lamy syndrome
Menkes disease
Metachromatic Leukodystrophy
3-Methylcrotonyl-CoA carboxylase deficiency
3-Methylglutaconic aciduria 1
Mevalonate kinase deficiency/aciduria
2-methylbutyryl CoA deficiency
Methylmalonic acidemia
Methylmalonyl-CoA mutase deficiency
Mitochondrial trifunctional protein deficiency
Morquio syndrome
Mucolipidosis (all types)
Mucopolysaccharidoses disorders
Mulibrey nanism
Multiple Sclerosis
Multiple sulfatase deficiency
Multiple system atrophy
Muscular dystrophy
Myelopathy
Myotonia congenita
Narcolepsy/cataplexy
N-Acetylglutamate synthase deficiency
Neonatal adrenoleukodystrophy
Nephropathy/Glomeronephritis
Neurological Visual Impairment
Neuromyelitis optica
Neuronal Ceroid Lipofuscinoses
Niemann-Pick Disease
Nonketotic hyperglycinemia
Northern Epilepsy syndrome
Obstructive lung disease
Ocular albinism
Optic Nerve Hypoplasia
Ornithine carbamoyltransferase deficiency
Osteomyelitis
Parkinson’s disease
Pemphigus
Pelizaeus–Merzbacher disease
Peripheral arterial diseases
Periventricular leukomalacia
Peroxisomal disorder
Peroxisome biogenesis disorders
Pervasive developmental disorder
Phenylketonuria
Pipecolic acedemia/ Hyperpipecolatemia
Polymyositis
Pompe’s disease
Porphyria cutanea tarda
Porphobilinogen synthase Deficiency
Primary biliary cirrhosis
Primary carnitine deficiency
Progressive supranuclear palsy
Prolidase deficiency
Propionic acidemia
Pseudo-Hurler polydystrophy
Psoriasis
Psoriatic arthritis
Pulmonary diseases
Pycnodysostosis
6-Pyruvoyltetrahydropterin synthase deficiency
Radiation injuries (Post radiation injuries)
Radiation induced lung injury
Reactive arthritis, Reiter’s sd
Red cell aldolase deficiency
Refsum disease
Reiter's syndrome
Restrictive lung disease
Retinitis Pigmentosa
Retinopathy
Rett syndrome
Rheumatism
Rheumatoid arthritis
Rhizomelic chondrodysplasia punctata
Rotor syndrome
Saccharopinuria
Salla disease
Sandhoff disease
Sanfilippo syndrome
Santavuori-Haltia syndrome
Scheie Syndrome
Schindler disease
Scleroderma
Sialidosis
Sideroblastic anemia
Sjögren syndrome
Sly Syndrome
Spastic diplegia
Spinal Muscular Atrophy
Stargardt's Disease
Sturge-Weber Syndrome
Stroke
Systemic lupus erythematosus
Tangier disease
Tarui’s disease
Tay-Sachs disease
Tetrahydrobiopterin deficiency
Thermal radiation injury
Trimethylaminuria/ fish odor syndrome
Tyrosinemia
Ulcerative Colititis
Urocanic aciduria
Usher Syndrome
Variegate porphyria
Vitelliform macular dystrophy
Vitiligo
Von Gierke’s disease
Von Willebrand disease
Waardenburg syndrome
Werdnig-Hoffman disease (SMA)
Wilson’s disease
Wolman disease
X-linked adrenoleukodystrophy
Zellweger syndrome
 

 

We are here to help you!

Click the Contact Us button and you will get all your answers and a chance to a new, healthy life!

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Disclaimer Stem Cell Therapy

Qualifications

regentim stem cell therapy clinic lebanon beirut europe middle east title

 

regentime stem cell therapy clinic lebanon beirut Nassim Abi Chahine doctor neurosurgeon

Dr. Nassim Abi Chahine, M.D, has a medical background in Neurosurgery. He established Regentime with the plan of hlping patients with their incurable diseases and to give hope for their recovery and treatment.
His work has broadened nationwide with much success and it is still growing. Dr. Nassim travels continuously abroad taking part at seminars and conferences to find out about the new developments in the stem cell therapy industry and to bring innovation to his clinic.

Dr. Abi Chahine is a highly experienced and professional surgeon, but at the same time friendly and open to the patients' questions, explaining to each and every one of them how Regentime treatments work and how they can help with their medical conditions.

Physician’s profile

General Neurosurgeon

 

Languages

English, Arabic, French, Polish, Spanish, Russian, Italian.

 

 

Education

Saint George Hospital University Medical Center, Beirut Lebanon

University of Balamand, Beirut Lebanon

The Medical Academy of Lodz, Poland

The Medical University of Lodz, Poland

 

About

Born in Koura North Lebanon in 1977, the doctor has a high professional performance in neurosurgery. He is known for his Heparin use in intraventricular haematoma treatment; a life saving technique since 2009. He established Regentime with the plan of helping patients with their incurable diseases. His work has broadened nationwide with much success and it is still growing.

Dr Nassim Abi Chahine travels continuously abroad, taking part at seminars and conferences to find out about the new developments in the stem cell therapy industry.

Dr. Abi Chahine is a highly experienced and professional neurosurgeon. He is very friendly and open to patients’ questions.

Areas of Expertise

Brain Surgery
Peripheral Nerve Surgery
Spine Surgery
 

Publications

1.      Success of heparin use in intraventricular haematoma treatment, Oct 2009
2.      Kyphoplasty, state-of-the-art, Oct 2008
3.      First global case of brain abscess caused by Kluyvera, April 2008
4.      Dandy-Walker malformation: Surgical treatment of 17 cases, Apr 2008
5.      A rare etiology of myelopathy: Spinal dural arterio-venous fistula, Oct 2007
6.      Spinal extradural arachnoid cysts,  Apr 2007

 

Membership

- Moderator of the MedHelp International Neurosurgery forum.
- Member of the Walter E. Dandy Neurosurgical Society The society for operative neurosurgery.
- Member of WALN, the World Association of Lebanese Neurosurgeons.
- Cofounder of the WALN-Young Neurosurgeon Committee.
- Member of the Lebanese Society of Neurosurgery.
- Member of The Resident Teaching Committee at Saint Georges Hospital Beirut.

 

We are here to help you!

Click the Contact Us button and you will get all your answers and a chance to a new, healthy life!

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Testimonials

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regentime regenerative cell therapy clinic lebanon beirut testimonial after stem cell image

Zuheir's success story

Letter from mother of Zuheir (Autism)  5 year old, Jordan


Hello Dr. Nassim,
We are all fine thank you, and Zuhair has no more headache..Thanks God.
We measured the improvement in every aspect; we think he has improvements so far as follows:
1- Eye contact 90% improvement (No longer avoiding looking at faces)
2- Response to his name 80% improvement (Usually no response when called by his name)
3- Communication with family 80% improvement (Now likes to be among us following his dad where he goes and pulls me to follow)
4- Concentration 60% improvement (Now notices who is coming, foreign people and parents when leaving)
5- Cognition 50% improvement (Starts to laugh at comedy cartoon scenes on TV and notices people and things through the car window)
6- Receptive language 30% improvement (Starts to understand few more words and commands)
7- Social interaction 20%  (Looks at thing with other people, at children playing, and now he follows them where they go)
8- Stuttering 10% improvement (Still flaps his arms/hands, teeth grinding and stuttering decreased slightly)
9- Properly playing 10% improvement (Started holding real toys, decrease in no-meaningful attachment to things e.g. wire, rope...)
10- Speech 1% (He’s trying to say new letters never said before)

 

We are here to help you!

Click the Contact Us button and you will get all your answers and a chance to a new, healthy life!

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Disclaimer Stem Cell Therapy

Awards

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We are here to help you!

Click the Contact Us button and you will get all your answers and a chance to a new, healthy life!

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Location

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We are here to help you!

Click the Contact Us button and you will get all your answers and a chance to a new, healthy life!

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